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IEC 60601 Electrical Safety Testing Service (Leakage/Ground) in Equatorial Guinea
Engineering Excellence & Technical Support
IEC 60601 Electrical Safety Testing Service (Leakage/Ground) High-standard technical execution following OEM protocols and local regulatory frameworks.
Rigorous Leakage Current Testing
Our IEC 60601 compliant leakage current testing in Equatorial Guinea meticulously measures earth, enclosure, and patient leakage to ensure your medical devices prevent hazardous current flow, safeguarding both patients and operators.
Comprehensive Grounding Integrity Verification
We perform thorough ground continuity tests according to IEC 60601 standards, verifying the effectiveness of your medical equipment's protective earthing. This is critical for fault current dissipation and preventing electric shock in Equatorial Guinea's operational environments.
IEC 60601 Certified Compliance for Equatorial Guinea
Leveraging our expertise, we provide IEC 60601 electrical safety testing, including leakage and ground integrity, specifically tailored for the regulatory landscape of Equatorial Guinea. Our service ensures your medical devices meet international safety benchmarks.
What Is Iec 60601 Electrical Safety Testing Service (Leakage/ground) In Equatorial Guinea?
IEC 60601 electrical safety testing, specifically focusing on leakage current and protective earth (ground) continuity, is a critical regulatory requirement for medical electrical equipment (MEE) intended for use in Equatorial Guinea. This service ensures that MEE devices do not pose an unacceptable risk of electric shock to patients or operators under normal and single-fault conditions. The testing adheres to the standards outlined in the IEC 60601 series, which are internationally recognized benchmarks for medical device safety. Leakage current refers to the unintended flow of electrical current from the device's live parts to accessible conductive surfaces or to earth. Protective earth continuity verifies that the grounding path within the device is robust and effectively dissipates any fault currents to ground, preventing hazardous voltage buildup on accessible parts. This service is a mandatory part of the conformity assessment process for MEE entering or being manufactured within Equatorial Guinea, requiring manufacturers and importers to demonstrate compliance.
| Who Needs IEC 60601 Leakage/Ground Testing in Equatorial Guinea? | Typical Use Cases for IEC 60601 Leakage/Ground Testing | ||||
|---|---|---|---|---|---|
| Manufacturers of Medical Electrical Equipment (MEE): Developing MEE for the Equatorial Guinean market. | Importers and Distributors of MEE: Bringing foreign-manufactured MEE into Equatorial Guinea. | Service and Maintenance Providers: Conducting repairs or modifications on existing MEE that may affect its electrical safety. | Original Equipment Manufacturers (OEMs): Incorporating MEE components into larger medical systems. | Regulatory Bodies: Used by authorities for market surveillance and post-market control. | |
| Diagnostic Imaging Equipment: X-ray machines, CT scanners, MRI machines, ultrasound devices. | Patient Monitoring Systems: ECG monitors, blood pressure monitors, pulse oximeters. | Therapeutic Devices: Infusion pumps, ventilators, dialysis machines, electrosurgical units. | Surgical Instruments: Electrically powered surgical tools, endoscopes. | Laboratory Equipment: Analyzers, centrifuges with electrical components. | Rehabilitation Equipment: Electrically powered physical therapy devices. |
Key Aspects of IEC 60601 Leakage/Ground Electrical Safety Testing:
- Leakage Current Testing: Assesses capacitive and resistive leakage currents under various operating conditions (normal, single fault). Measurements are taken for earth leakage, enclosure (chassis) leakage, and patient leakage (applied parts).
- Protective Earth Continuity Testing: Evaluates the integrity and resistance of the protective earth connection. This ensures that in the event of an internal fault, the grounding system can safely conduct fault current without creating a dangerous voltage on accessible conductive parts.
- Dielectric Strength (Hi-Pot) Testing (often performed in conjunction): While not strictly 'leakage/ground' in isolation, Hi-Pot testing is a related safety test that verifies the insulation's ability to withstand high voltages, preventing breakdown and potential arcing.
- Compliance Documentation: Successful completion of these tests results in a test report that serves as evidence of compliance with IEC 60601 standards.
- Regulatory Alignment: Ensures MEE meets the safety requirements stipulated by Equatorial Guinean regulatory bodies for market access.
Who Needs Iec 60601 Electrical Safety Testing Service (Leakage/ground) In Equatorial Guinea?
IEC 60601 electrical safety testing, specifically focusing on leakage current and ground continuity, is a critical requirement for ensuring the safety of medical devices. In Equatorial Guinea, the demand for these services primarily stems from entities that import, manufacture, or operate medical equipment. Compliance with this international standard is essential for market access, patient safety, and regulatory adherence. The need is driven by the inherent risks associated with electrical medical devices, where faulty grounding or excessive leakage current can lead to electric shock, equipment malfunction, and harm to both patients and healthcare professionals.
| Target Customer/Department | Reason for Needing IEC 60601 Testing (Leakage/Ground) | Key Responsibilities/Interests |
|---|---|---|
| Medical Device Importers and Distributors | To ensure imported medical devices meet international safety standards for sale and distribution in Equatorial Guinea. Facilitates market entry and prevents rejection by regulatory authorities. | Importation compliance, distribution network safety, product certification, regulatory liaison. |
| Manufacturers of Medical Devices (if any local manufacturing) | To guarantee that locally manufactured medical devices are safe for use and comply with international electrical safety requirements before sale and deployment. | Product design and development, manufacturing quality control, product certification, market access. |
| Hospitals and Healthcare Facilities (Public and Private) | To ensure the safety of the medical equipment used within their facilities, protecting patients and staff from electrical hazards. Essential for maintaining patient care standards and avoiding liability. | Equipment procurement, patient safety, staff safety, risk management, regulatory compliance, equipment maintenance. |
| Clinics and Diagnostic Centers | Similar to hospitals, these facilities rely on safe medical equipment for patient diagnosis and treatment. Ensures operational continuity and patient trust. | Equipment acquisition, patient well-being, operational efficiency, compliance with local health regulations. |
| Government Health Ministries and Regulatory Bodies | To establish and enforce medical device safety regulations, ensuring that only compliant and safe equipment enters and operates within the country. Crucial for public health and patient protection. | Policy development, regulatory oversight, market surveillance, enforcement of standards, public health protection. |
| Procurement Departments within Healthcare Institutions | To specify and verify that purchased medical equipment meets the necessary safety certifications, including IEC 60601, as part of the tender and acquisition process. | Tender evaluation, supplier vetting, contract specifications, budget adherence, acquisition of safe equipment. |
| Biomedical Engineering Departments | Responsible for the installation, maintenance, and repair of medical equipment. They perform or oversee regular safety testing to identify and rectify potential electrical hazards. | Equipment installation, preventive maintenance, corrective maintenance, safety testing, equipment lifecycle management. |
| Quality Assurance and Compliance Departments | To ensure that all medical devices within the organization meet internal and external safety and regulatory requirements. They often manage the documentation and verification of safety testing. | Policy implementation, audit preparation, documentation management, risk assessment, regulatory adherence. |
Target Customers and Departments Requiring IEC 60601 Electrical Safety Testing (Leakage/Ground) in Equatorial Guinea
- Medical Device Importers and Distributors
- Manufacturers of Medical Devices (if any local manufacturing)
- Hospitals and Healthcare Facilities (Public and Private)
- Clinics and Diagnostic Centers
- Government Health Ministries and Regulatory Bodies
- Procurement Departments within Healthcare Institutions
- Biomedical Engineering Departments
- Quality Assurance and Compliance Departments
Iec 60601 Electrical Safety Testing Service (Leakage/ground) Process In Equatorial Guinea
This document outlines the typical workflow for IEC 60601 electrical safety testing services, specifically focusing on leakage and ground testing, for medical devices within Equatorial Guinea. The process is designed to ensure compliance with international safety standards and facilitate market access for manufacturers. The workflow spans from initial client inquiry to the final delivery of test reports and certifications.
| Stage | Key Activities | Deliverables | Equatorial Guinea Relevance |
|---|---|---|---|
| Inquiry & Consultation | Initial contact, understanding device & scope, discuss standards (IEC 60601-1) | Initial consultation notes, understanding of requirements | Establishes the foundation for compliance relevant to the Equatorial Guinean market. |
| Quotation & Agreement | Formal quote, service agreement, pricing, timelines | Signed quotation/contract | Legal framework for testing services targeting Equatorial Guinean market access. |
| Documentation Submission | Provide technical specs, manuals, BOM, intended use | Submitted documentation package | Information required for testing applicable to devices intended for use in Equatorial Guinea. |
| Sample Submission | Ship medical device samples | Received device samples | Physical devices to be tested for compliance with standards required in Equatorial Guinea. |
| Test Plan Development | Create detailed test plan for leakage/ground tests (IEC 60601) | Approved test plan | Specifies the exact tests ensuring safety for patients and operators in Equatorial Guinea. |
| Testing Execution | Perform earth bond, touch current, patient leakage, insulation resistance tests | Raw test data, test logs | Critical safety verification of the device intended for the Equatorial Guinean healthcare system. |
| Report Generation | Analyze data, compile comprehensive test report | Draft test report | Documented evidence of safety compliance for regulatory purposes in Equatorial Guinea. |
| Report Issuance | Internal review, issue final report | Final IEC 60601 test report | Official document for submission to Equatorial Guinean regulatory bodies. |
| Certification & Market Access | Issue certificate (if applicable), provide guidance | Certificate of Conformity (optional), market access advice | Facilitates the legal entry and sale of the medical device in Equatorial Guinea. |
IEC 60601 Electrical Safety Testing (Leakage/Ground) Process - Equatorial Guinea
- 1. Initial Inquiry & Consultation:
- Client contacts a recognized testing laboratory or certification body with a request for IEC 60601 leakage and ground testing for their medical device(s).
- The laboratory provides an initial consultation to understand the device, its intended use, target markets, and relevant IEC 60601 standards (e.g., IEC 60601-1 and relevant collateral/particular standards).
- Discussion of project scope, timelines, and preliminary cost estimates.
- 2. Quotation & Agreement:
- Based on the consultation, the laboratory issues a formal quotation detailing the scope of work, testing procedures, fees, and estimated turnaround time.
- Client reviews and accepts the quotation. A formal service agreement or contract is signed.
- 3. Pre-Testing Information & Documentation Submission:
- The client submits essential documentation to the laboratory, which typically includes:
- Device technical specifications and schematics.- User manuals and service manuals.- Bill of Materials (BOM).- Previous test reports (if any).- Information on intended use and classification of the device.- Any specific national requirements for Equatorial Guinea (if known and provided by the client).- 4. Sample Submission:
- The client ships the required number of representative samples of the medical device to the laboratory's designated testing facility.
- Clear labeling and identification of samples are crucial.
- 5. Pre-Compliance Assessment (Optional but Recommended):
- The laboratory may offer a pre-compliance assessment to identify potential issues before formal testing, saving time and cost.
- 6. Test Plan Development & Review:
- The laboratory develops a detailed test plan based on the submitted documentation and the relevant IEC 60601 standards.
- The test plan outlines specific tests to be performed, including:
- **Earth/Ground Bond Resistance Testing:** Verifies the integrity of the protective earth connection.- **Touch Current Testing:** Measures the leakage current that can flow through a person touching accessible parts of the device.- **Patient Leakage Current Testing:** Measures leakage current flowing from applied parts to earth or accessible conductive parts.- **Insulation Resistance Testing:** Assesses the quality of insulation between conductive parts.- The test plan may be shared with the client for review and approval.
- 7. Formal Testing Execution:
- The laboratory's trained technicians conduct the tests in a controlled environment using calibrated equipment.
- Tests are performed according to the approved test plan and relevant IEC 60601 standards.
- All test parameters, results, and observations are meticulously recorded.
- 8. Data Analysis & Report Generation:
- The test data is analyzed by the laboratory's engineering team.
- A comprehensive test report is compiled, which includes:
- Executive summary.- Device description and identification.- Standards applied.- Test setup and conditions.- Detailed test results for leakage and ground tests.- Compliance statements.- Photographs of the device and test setups.- Any deviations or remarks.- 9. Report Review & Issuance:
- The test report is reviewed internally by the laboratory.
- The final report is issued to the client.
- 10. Certification & Market Access Support:
- Upon successful completion of testing and satisfactory results, the laboratory may issue a certificate of conformity or a similar document, depending on their accreditation and the client's requirements.- This report and certificate serve as evidence of compliance with IEC 60601 electrical safety standards, crucial for medical device registration and market access in Equatorial Guinea (and other regions adhering to these standards).- The laboratory may provide guidance on the regulatory submission process for Equatorial Guinea, if required.- 11. Record Keeping & Post-Certification Support:
- The laboratory maintains records of the testing and reports for a specified period.- The client should retain these reports for their own records and future regulatory submissions. Any post-market surveillance or re-evaluation requirements may necessitate future testing.
Iec 60601 Electrical Safety Testing Service (Leakage/ground) Cost In Equatorial Guinea
IEC 60601 electrical safety testing, specifically focusing on leakage and ground (protective earth) current measurements, is a critical compliance requirement for medical devices intended for the market in Equatorial Guinea. While there isn't a publicly published, standardized fee schedule for these specific tests in Equatorial Guinea, the cost is influenced by several factors. These include the complexity of the device, the number of test points required, the testing laboratory's accreditation and reputation, and the turnaround time requested. Generally, testing will be conducted by accredited third-party laboratories, either locally if available and competent, or more likely through regional or international laboratories that service Equatorial Guinea. The cost will be presented in the local currency, the Central African CFA franc (XAF).
| Testing Component | Estimated Cost Range (XAF) | Notes |
|---|---|---|
| IEC 60601 Leakage Current Testing (e.g., Earth Leakage, Enclosure Leakage, Patient Leakage) | 200,000 - 800,000 XAF per device/configuration | This range is a broad estimate. Highly complex devices or multiple configurations will be at the higher end. May include multiple subtypes of leakage testing. |
| IEC 60601 Ground/Protective Earth Continuity Testing | 150,000 - 400,000 XAF per device | Assesses the effectiveness and integrity of the protective earthing system. Cost depends on the number of earth points and complexity. |
| Combined Leakage & Ground Testing Package | 300,000 - 1,200,000+ XAF per device | Often bundled. The higher end reflects comprehensive testing across all relevant standards and device modes. This is a typical scenario for full compliance. |
| Report Generation and Documentation | Included in above, or additional 50,000 - 150,000 XAF | Detailed reports are crucial for regulatory submission. May be a separate charge for basic reporting vs. comprehensive certification-level reports. |
Factors Influencing IEC 60601 Leakage/Ground Testing Costs in Equatorial Guinea:
- Device Complexity: More complex devices with multiple power inputs, accessories, or diverse operational modes will require more extensive testing, increasing the overall cost.
- Number of Test Points: The number of distinct configurations and operating modes of the medical device that need to be tested for leakage and ground current contributes to the testing duration and thus the price.
- Laboratory Accreditation and Reputation: Laboratories with international accreditations (e.g., ISO 17025) and a strong track record may command higher fees.
- Turnaround Time: Expedited testing services typically incur additional charges.
- Scope of Testing: While focusing on leakage and ground, sometimes these tests are part of a broader IEC 60601 compliance assessment, which would affect the total project cost.
- Travel and Logistics: If testing is outsourced to a lab not physically located in Equatorial Guinea, costs for shipping samples, engineer travel (if required), and associated logistics will be factored in.
- Reporting Requirements: The detail and formality of the test report can also influence the cost.
Affordable Iec 60601 Electrical Safety Testing Service (Leakage/ground) Options
Our affordable IEC 60601 electrical safety testing service provides essential leakage and ground bond testing for medical devices. We understand the critical need for compliance without breaking the bank. We offer flexible options and value bundles designed to maximize your return on investment and minimize your testing costs. Our streamlined process and experienced technicians ensure efficient and accurate results, helping you bring your products to market faster and more cost-effectively. Prioritizing safety doesn't have to be expensive.
| Value Bundle Name | Description | Included Tests | Typical Devices | Cost-Saving Benefits | Price Indicator (Starting From) |
|---|---|---|---|---|---|
| Essentials Package | Our most budget-friendly option, focusing on the core safety requirements. | Leakage Current (Earth, Enclosure, Patient, Patient Auxiliary), Protective Earth Resistance (Ground Bond). | Low-risk medical devices, accessories, components. | Reduced per-test cost, ideal for initial product development or low-volume production. | $XXX per device/batch |
| Standard Compliance Bundle | Comprehensive testing for most standard medical devices requiring IEC 60601-1 compliance. | Includes all tests from the Essentials Package, plus applied parts testing. | Diagnostic equipment, patient monitoring devices, basic therapeutic devices. | Better value for multiple tests, streamlined reporting, predictable budgeting. | $YYY per device/batch |
| High-Volume Production Pack | Designed for manufacturers with consistent, large-scale production runs. | All standard compliance tests, with options for custom test plans and expedited reporting. | High-volume consumables, mass-produced medical equipment. | Significant per-unit cost reduction, dedicated scheduling, bulk discounts. | Custom Quote - Contact Us |
| Component Qualification Bundle | Testing for individual components to ensure they meet safety standards before integration. | Focuses on specific leakage and ground bond requirements relevant to the component. | Power supplies, connectors, internal circuitry. | Proactive risk mitigation, prevents costly redesigns later, reduces testing on finished products. | $ZZZ per component type |
Why Choose Our Affordable IEC 60601 Testing?
- Cost-Effective Solutions: Competitive pricing and smart bundling to fit your budget.
- Essential Safety Compliance: Focus on critical leakage and ground bond tests (IEC 60601-1).
- Experienced Technicians: Ensuring accuracy and efficiency in testing.
- Faster Turnaround Times: Helping you meet your product launch deadlines.
- Reduced Risk: Ensuring your devices meet international safety standards.
- Scalable Services: Options for small batches to larger production runs.
Verified Providers In Equatorial Guinea
Ensuring access to quality healthcare in Equatorial Guinea requires a keen understanding of which providers are not only licensed but also adhere to the highest standards of medical practice. Franance Health stands out as a beacon of trust and excellence in this landscape. Their commitment to rigorous credentialing, continuous professional development, and patient-centric care makes them a top-tier choice for anyone seeking reliable medical services.
| Credential Verification | Expertise & Specializations | Patient Care Philosophy | Regulatory Compliance |
|---|---|---|---|
| Extensive checks of medical degrees, licenses, and certifications from accredited institutions. | Access to a diverse pool of specialists with proven track records in various medical fields. | Emphasis on empathetic communication, personalized treatment plans, and patient empowerment. | Strict adherence to Equatorial Guinean healthcare regulations and international best practices. |
| Verification of prior work experience and professional references. | Ongoing training programs to ensure medical staff are at the forefront of medical innovation. | Commitment to privacy and confidentiality of patient records. | Regular audits and quality assurance checks to maintain service excellence. |
Why Franance Health Excels as a Verified Provider:
- Rigorous Credentialing Process: Franance Health employs an exhaustive verification process for all their medical professionals. This includes thorough background checks, validation of educational qualifications and licenses from recognized international and national bodies, and meticulous review of professional experience.
- Adherence to International Standards: Beyond local regulations, Franance Health aligns its practices with internationally recognized medical protocols and ethical guidelines, ensuring a high level of care that meets global benchmarks.
- Continuous Professional Development: The organization prioritizes ongoing training and education for its staff, keeping them updated with the latest medical advancements, technologies, and best practices. This commitment guarantees that patients receive care informed by current medical knowledge.
- Patient Safety and Ethical Practice: Franance Health places paramount importance on patient safety and upholds the highest ethical standards in all its operations. This translates to transparent communication, informed consent, and a dedication to patient well-being.
- Comprehensive Service Offerings: Franance Health offers a broad spectrum of medical services, catering to diverse healthcare needs, from primary care to specialized treatments, all delivered by qualified and verified professionals.
- Commitment to Accessibility: While maintaining high standards, Franance Health also strives to make quality healthcare accessible to a wider population within Equatorial Guinea, understanding the unique challenges of the region.
Scope Of Work For Iec 60601 Electrical Safety Testing Service (Leakage/ground)
This Scope of Work (SOW) outlines the requirements for Electrical Safety Testing services, specifically focusing on Leakage Current and Grounding (Continuity) tests, as per the IEC 60601 series of standards. The service will ensure medical electrical equipment meets the stringent safety requirements necessary for patient and operator protection. This document details the technical deliverables, applicable standard specifications, and testing methodologies.
| Test Type | Standard Specification | Test Description | Acceptance Criteria (Typical) |
|---|---|---|---|
| Grounding (Continuity) Test | IEC 60601-1 (e.g., Clause 8.4, 8.5) | Measures the resistance of the protective earth conductor and connections to ensure a low-impedance path to ground. This prevents dangerous voltages from appearing on accessible conductive parts in case of a fault. | Resistance typically < 0.1 Ohm (dependent on cable length and device characteristics, as per standard). |
| Enclosure Leakage Current (Earth) | IEC 60601-1 (e.g., Clause 11.5) | Measures the current flowing through the protective earth conductor when the equipment is operated under normal and single-fault conditions. This ensures the integrity of the protective earthing system. | Typically < 10 mA (for Class I equipment) under normal conditions; < 50 mA under single-fault conditions (as per standard). |
| Enclosure Leakage Current (Direct Contact) | IEC 60601-1 (e.g., Clause 11.5) | Measures the current that can flow through a person touching accessible conductive parts under normal and single-fault conditions. This assesses the risk of electric shock to the patient. | Typically < 0.1 mA (Type B), < 0.01 mA (Type BF), < 0.001 mA (Type CF) under normal conditions; limits increase under single-fault conditions (as per standard). |
| Enclosure Leakage Current (Indirect Contact) | IEC 60601-1 (e.g., Clause 11.5) | Measures the current that can flow through a person touching accessible conductive parts under normal and single-fault conditions. This assesses the risk of electric shock to an operator or caregiver. | Typically < 0.5 mA under normal conditions; limits increase under single-fault conditions (as per standard). |
| Patient Leakage Current (Direct) | IEC 60601-1 (e.g., Clause 11.5) | Measures the current that can flow through a patient from applied parts to earth under normal and single-fault conditions. This is critical for patient safety, especially for applied parts in direct contact with the patient. | Typically < 0.1 mA (Type B), < 0.01 mA (Type BF), < 0.001 mA (Type CF) under normal conditions; limits increase under single-fault conditions (as per standard). |
| Patient Leakage Current (Indirect) | IEC 60601-1 (e.g., Clause 11.5) | Measures the current that can flow through a patient from applied parts to other conductive parts of the patient under normal and single-fault conditions. This assesses the risk of current circulating within the patient. | Typically < 0.5 mA under normal conditions; limits increase under single-fault conditions (as per standard). |
Key Objectives and Deliverables
- To perform comprehensive Leakage Current and Grounding (Continuity) testing on the specified medical electrical equipment.
- To verify compliance with relevant clauses of IEC 60601-1 and applicable collateral/particular standards.
- To provide detailed test reports documenting all test results, methodologies, and any observed deviations or non-conformities.
- To offer recommendations for remediation in case of identified non-compliance.
- To ensure the electrical safety of the medical electrical equipment for its intended use.
Service Level Agreement For Iec 60601 Electrical Safety Testing Service (Leakage/ground)
This Service Level Agreement (SLA) outlines the guaranteed response times and uptime for the IEC 60601 Electrical Safety Testing Service, specifically focusing on Leakage and Ground testing, provided by [Your Company Name]. This SLA is applicable to all clients who have subscribed to this service.
| Service Component | Service Level Objective (SLO) | Measurement Metric | Reporting Frequency |
|---|---|---|---|
| Initial Response to Service Request (Leakage/Ground Test) | A qualified technician will acknowledge and begin assessment of your service request within 4 business hours. | Time from service request submission to initial technician contact. | Real-time notification for urgent requests, daily for standard requests. |
| On-Site Service Commencement (Remote Support not applicable) | For on-site testing, a technician will be dispatched and arrive at the client's location within 2 business days of request confirmation (subject to travel feasibility and scheduling). | Time from request confirmation to technician arrival. | Weekly reporting on dispatched requests. |
| Test Completion Time | Standard Leakage/Ground testing for up to 5 devices will be completed within 1 business day after on-site arrival. Larger batches will be quoted separately. | Time from technician arrival to completion of scheduled tests. | End-of-testing report. |
| Uptime Guarantee for Testing Equipment | The availability of our testing equipment and platform for scheduled and on-demand testing is guaranteed at 99.5% per calendar month. | Percentage of time the testing service is operational and accessible. | Monthly Uptime Report. |
| Report Delivery | Comprehensive test reports will be delivered electronically within 1 business day of test completion. | Time from test completion to report delivery. | End-of-testing report. |
| Re-testing due to Failed Initial Test | If a device fails initial testing, re-testing after necessary repairs or adjustments will be scheduled within 1 business day of notification of readiness for re-test. | Time from notification of repair readiness to commencement of re-test. | As needed, reported with final pass/fail. |
Scope of Service
- IEC 60601-1 compliance testing for electrical safety.
- Leakage Current Testing (Earth Leakage, Touch Current, Patient Leakage).
- Ground Continuity / Protective Earth Testing.
- Documentation and reporting of test results.
- Provision of calibrated test equipment.
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