Buy MRI Injector System (Contrast) in Nigeria.

Which MRI injector systems can I buy in Nigeria?

The current Franance category has two assigned records: Bayer MEDRAD MRXperion and Bayer MEDRAD Spectris Solaris EP. MRXperion is the current manufacturer product page represented in the catalogue. Spectris Solaris EP is a legacy family that Bayer lists in a product-lifecycle notice. Its presence helps a facility identify a system or discuss an existing installed unit; it does not mean a new unit or a particular service package is available.

The listing count is deliberately precise: two records assigned to this category, not a complete inventory of every MRI injector on the market. The records are Bayer models and do not imply that all MRI scanners, agents, accessories or rooms are compatible with either system. Use the listing to identify the model you want reviewed, then state your scanner and facility requirements in the quotation request.

You can also view the Bayer MRXperion listing within the Bayer and MRI-injector combination, or return to the wider MRI systems category. An injector is a separate piece of suite equipment; it is not automatically included with an MRI scanner purchase.

What does an MRI contrast injector do?

An MRI power injector is a syringe-based fluid delivery system designed for use during MRI applications. Bayer describes MRXperion as delivering MR contrast media and saline, with a separate scan-room unit and workstation components. The injector may also support stored protocols, data documentation and optional connection to a scanner, depending on the model and configuration. The exact workflow and device functions must be confirmed in the current instructions for use for the offered unit.

The equipment is only one part of a contrast-enhanced MRI workflow. A facility must separately establish its clinical protocol, staffing, patient screening, agent selection, dose, route and monitoring under professional governance. This page is not a clinical protocol and does not recommend whether a patient should receive contrast or how an injection should be programmed. Bayer states that trained healthcare professionals are intended to operate MRXperion; use the product documentation and the institution’s approved procedures.

For purchasing, focus on what the equipment package actually contains: injector head or scan-room unit, workstation, power supply, mounting hardware, communication modules, software, syringe kits and other accessories. A product-family description does not prove every component is included in a specific quotation. Ask for an itemised scope and the model or part number for each quoted component.

How do MRXperion and Spectris Solaris EP differ?

MRXperion is the newer MR injector reference in this category. Bayer’s page describes MRXperion’s intended MR use, available connectivity features, MR Conditional status and system capabilities. Its published specifications include 65 mL contrast and 115 mL saline syringe capabilities, a programmable flow range of 0.01–10 mL/s, and storage for 60 protocols with up to six phases each. Those specifications describe this model and do not select a patient protocol or establish what Franance can supply in Nigeria.

Bayer lists MRXperion scanner-field-strength support up to and including 7 Tesla, optional ISI2 scanner connectivity and a mobile clamp option. The same page states that the scan-room unit and power supply are MR Conditional only under specified conditions of use. The field-strength statement does not replace checking equipment placement, separation, orientation, access restrictions, software, scanner interface or manual conditions for the exact proposed configuration.

Spectris Solaris EP is a legacy MR injector family. Bayer’s lifecycle page lists fixed and mobile versions with an end-of-life date of December 31, 2028. Bayer says that after the applicable end-of-life date it no longer offers service, calibration, replacement parts, technical support or consumables for the affected installed base. Before considering this entry, ask Franance to verify current offerability, the exact version and condition, documentation, parts and disposable status, and any support terms that can be confirmed in writing. Do not treat the published lifecycle date as evidence that a specific offer will remain serviceable until then.

The MRXperion filtered listing and Spectris Solaris EP filtered listing lead to the two category records. They are different model families; interchangeable parts, accessories, syringes or software must not be assumed.

Why is an MRI injector different from a CT injector?

MRI and CT injectors are not interchangeable just because both deliver contrast under a programmed protocol. MRI rooms contain a strong magnetic field and create a specific equipment environment. A system used in or near that environment needs model-specific MR safety documentation and must remain within its stated conditions. A CT injector label, a general claim of “compatible,” or another unit’s MR Conditional status is not evidence that an injector is suitable for a particular MRI room.

Bayer’s product catalogue separates its MRXperion MR system from its CT injector portfolio. That distinction matters when an organisation also operates CT: the CT suite, injector, consumables and accessory requirements belong to a separate equipment specification. Do not order or place a CT-only system in an MR area based on visual similarity, shared brand or the fact that both systems use contrast syringes.

For an MRI project, identify the exact MRI scanner model and field strength, planned room position, any mobile-scanner requirement, nearby control-room layout, and any intended data interface. Ask the MRI vendor or responsible MR safety personnel to review the proposed injector’s documentation. The final technical decision belongs to the institution’s qualified MRI and biomedical engineering personnel using the current product manual and local safety procedures.

How do I check MRI-room compatibility?

Start with the exact injector model and its current operation manual, not a broad product-family statement. Confirm the named MR status, the field strength and other conditions stated in the manual, the allowed location and orientation of each component, and any restrictions on use, movement, mounting or power supply. MR Conditional means safe only within the stated conditions; it is not a general approval for every MRI scanner, room or configuration.

Then match those conditions to the actual MRI suite. Record the scanner make and model, field strength, room configuration, intended injector location, whether the room or scanner is mobile, and the proposed route for the workstation and power components. If the injector is to communicate with the scanner, verify that the correct interface module, software version and scanner connection are offered and supported for that exact combination. Bayer describes ISI2 as an optional module, so do not assume it is part of the base unit.

The American College of Radiology’s 2026 Manual on MR Safety is written for MR practitioners, technologists, medical physicists, administrators and other healthcare professionals. It is a reference for institutional MR safety governance, not a substitute for the injector manual or a site-specific review. Ask the facility’s MR safety lead or designated qualified personnel to approve placement and operating conditions before acceptance. Keep the written compatibility confirmation with the equipment documentation.

What should I verify about syringes, tubing and contrast agents?

Ask for the manufacturer’s current compatibility list for the exact injector model, syringe kit, tubing set and agent presentation. Bayer publishes distinct syringe and disposable kits for its MRXperion and Spectris Solaris EP product families. A syringe listed for MRXperion does not become compatible with Spectris Solaris EP, a different Bayer injector or another manufacturer’s system by appearance alone. Confirm exact catalogue references and pack contents.

For MRXperion, Bayer says the operation manual contains the complete compatible-agent list. Use that list for the exact model and configuration; do not infer compatibility from an agent appearing in a marketing page, from a facility’s existing inventory, or from a similarly named CT product. The contrast agent’s clinical labeling and the facility’s clinical policy remain separate from this equipment procurement guide.

Specify whether the quotation should include contrast and saline syringe kits, connector tubing, spikes, check valves or any other required disposable. State whether the facility expects a single-use or multi-dose workflow only as a technical procurement requirement to be reviewed against manufacturer instructions. Ask the supplier to show what is included, what is optional and what must be procured separately. Have the clinical and biomedical teams verify the final references before use.

What scanner interface and documentation should I plan for?

Decide whether the facility needs standalone injector operation or a supported scanner interface. Bayer describes optional MRXperion connectivity, including ISI2, and lists workflow and documentation features such as protocol storage and output of injection information to systems such as PACS or RIS, subject to configuration. These features are not a guarantee that a particular hospital’s MRI scanner, information system, interface licence or network is supported. Verify exact system versions and the needed interface scope with the relevant vendors.

Prepare a simple interface schedule for the quotation: MRI manufacturer and model, software release where known, workstation arrangement, desired modality-worklist or scanner connectivity, PACS/RIS endpoint and any network or cybersecurity requirements. Ask which module, cable, software, licence, installation task or vendor coordination is included. If no interface is required, state that too so that the quote does not silently assume a connectivity package.

Request the current model-specific user manual, MR safety labelling, product datasheet, disposable references, electrical and dimensional information, warranty terms offered, and service documentation available for the actual market and offered configuration. For a legacy Spectris unit, add the unit’s serial number or exact version where available and ask specifically what lifecycle-related support remains. Local registration, import or facility requirements should be identified by the purchaser and verified with the responsible authorities; this guide does not claim a device has Nigerian approval.

How should a Nigerian facility plan the quote and installation scope?

Treat the quotation as a project specification, not a one-line request for an “MRI injector.” Confirm the scanner, field strength, room layout, mounting or mobility preference, intended injector location, workstation location, electrical supply, interface requirement, consumables and quantity. The facility should provide its actual site data; no generic Nigerian site condition can establish that a particular configuration fits a given suite.

If the request involves installation, identify the tasks that are expected: site survey, delivery into the facility, placement, configuration, scanner-interface testing, acceptance documentation and user training. Ask Franance to state whether each item is included, separately priced, excluded or dependent on another vendor. Neither a product listing nor a quotation enquiry by itself guarantees that a manufacturer technician, local engineer or service plan is available.

Plan the supply side as well as the equipment. Confirm the exact injector and accessory references, expected disposable replenishment, storage conditions from the applicable instructions, and who will own ongoing procurement. For a legacy product, ask whether the required consumables and spare parts can still be obtained for the proposed system and request a clear statement of their source and any limitations. Do not treat a lifecycle date as a promise of future stock.

In the enquiry, include the facility name, procurement contact, destination state and city, installation timeline requested, and any internal technical review deadline. This lets Franance reply against a defined Nigerian delivery destination and a specific scope rather than assuming nationwide stock or a delivery time.

What should I include in an MRI injector quotation request?

Include the exact product reference or the system under review, the desired quantity and whether the request concerns a new, replacement or installed legacy unit. Identify the MRI manufacturer, model, field strength and scanner software version if known. State whether the room/scanner is fixed or mobile, the required fixed or mobile injector format, the proposed scan-room placement and any clamp or mounting requirement.

List all requested components: scan-room unit, workstation, power supply, interface module, software or licence, syringe kits, tubing and accessories. Provide exact part numbers when the facility already has a validated specification. If it does not, ask for a technical review and a written compatibility response; do not ask the supplier to guess an MRI or clinical configuration from a broad description.

For Spectris Solaris EP, explicitly request confirmation of model/version, condition, current offerability, included consumables, technical documentation, parts status and support terms because Bayer classifies it as a legacy product family and publishes a lifecycle notice. For MRXperion, identify which optional interface, mounting, documentation or accessory elements the facility requires. Ask the quote to state all inclusions, exclusions, substitution details, condition, quoted delivery assumptions, commercial validity, warranty and any service or training scope.

Finally, give the destination city and state in Nigeria, quantity, preferred contact method and timing for a response. Attach the facility’s approved technical specification if available. Review the written proposal with procurement, biomedical engineering and the MR safety lead before accepting a configuration.

How do I buy an MRI contrast injector in Nigeria through Franance?

Choose a model from the MRI injector category, or send a quote request for Bayer MEDRAD MRXperion or a Spectris Solaris EP lifecycle enquiry. These contact links are quote enquiries, not checkout or payment links.

In your message, include the MRI and injector details, requested components, quantity, site city/state and the questions that need a written response. Franance follows up by phone or email after receiving the enquiry. The reply should establish the exact offer, any configuration caveats, commercial terms and delivery arrangements. Do not treat the product page as confirmation of a dispatch-ready unit or as clinical or MR safety approval.

Before approving an order, compare the written offer line by line with the facility specification. Confirm model and status, MR conditions, exact interface, included accessories, disposables, scope of installation or training, documentation and any declared warranty or service. Ask Franance to explain each deviation or substitution before the facility accepts it. The institution’s qualified staff retain responsibility for approving the equipment configuration and its use.

Frequently asked questions about MRI injectors in Nigeria

### Which MRI injectors does this category list?

The live category currently lists Bayer MEDRAD MRXperion and Bayer MEDRAD Spectris Solaris EP MR Injection System. These are two records, not an exhaustive inventory of every MRI injector. The Spectris Solaris EP record is a legacy reference and needs a current written offerability and support check.

### Can I use a CT injector in an MRI room?

Do not assume that a CT injector is MR suitable. Check the exact injector model’s MR safety labelling, operating manual and conditions against the MRI scanner and room. A CT designation, brand match or generic compatibility statement does not prove compatibility with an MR environment.

### Is MRXperion compatible with every scanner up to 7T?

Bayer’s page describes support for scanner field strengths up to and including 7T, while also identifying MR Conditional conditions and optional ISI2 connectivity. That headline does not confirm every MRI model, room placement, software version or interface. Verify the offered configuration in current instructions and obtain an explicit technical review.

### Is Spectris Solaris EP available as new equipment?

The catalogue cannot answer that. Bayer’s lifecycle page lists the MR and mobile MR systems with an end-of-life date of December 31, 2028. Ask Franance to confirm the exact unit’s offerability, condition, parts, consumables and support in writing.

### Can I buy it online?

No online checkout is provided. Submit a quotation enquiry; Franance follows up by phone or email. The enquiry does not itself confirm price, stock or a delivery date.

Manufacturer and safety references

- Bayer MEDRAD MRXperion MR Injection System - Bayer Product Lifecycle Announcements - Bayer injection-system syringe and disposable products brochure - American College of Radiology MR Safety resources and 2026 manual