Buy Ambu Mark IV Adult Resuscitator 304 002 000 in Nigeria
To buy the Ambu Mark IV Adult reusable manual resuscitator, product reference 304 002 000, in Nigeria, request a quotation from Franance and ask the supplier to confirm the full model reference and supplied configuration. Ambu identifies this reference as an adult Mark IV with two oxygen reservoir bags and one size 5 Ambu silicone face mask. The Mark IV is a manual resuscitator; the product is not a powered ventilator, oxygen source or complete emergency trolley. The adult model is specified for patients over 15 kg. It has a single-shutter patient valve and a swivel connector between the valve and mask. Ambu’s datasheet reports approximate resuscitator volume and delivered-volume figures under specified test conditions, but these are product specifications rather than a clinical result or a guarantee of delivered ventilation for every user, patient or setup. Selection and operation belong to trained healthcare professionals following the current instructions for use and local protocols.
Where can I buy Ambu Mark IV Adult 304 002 000 in Nigeria?
Franance handles this listing as a quotation order. Start with the exact filtered Ambu Mark IV Adult 304 002 000 listing, review the bag-valve-mask and manual resuscitator category, and request a Franance quotation for Ambu Mark IV Adult 304 002 000.
Include the number of units, facility type, delivery city and state, the exact reference, and any purchasing or documentation requirements. Ask the quote to identify the supplied product number, package contents, quotation validity, delivery arrangements and payment terms. Franance follows up by phone or email to clarify quotation requests; this is not an online checkout. A product’s presence on a manufacturer page or local listing does not establish Nigerian stock, delivery timing, local distributor status or price.
What is the Ambu Mark IV Adult resuscitator?
The Mark IV Adult is a reusable manual resuscitator designed for manual ventilation and resuscitation. Ambu describes the Mark IV family as available in Baby and Adult sizes. The specified adult version is for patients with a body weight greater than 15 kg. The product page describes a single-shutter valve system, a transparent patient-valve housing and a swivel connector between the valve and mask. Ambu says the transparent housing lets the user observe valve operation, while the swivel allows the resuscitator to change position relative to the mask.
Product reference 304 002 000 matters because the Mark IV name covers several package options. The manufacturer page lists 304 002 000 with two reservoir bags and one size 5 silicone face mask. Related codes are different kits: 304 004 000 lists the adult resuscitator with two reservoir bags but no mask in the item description, while 304 009 000 lists two reservoir bags and masks in sizes 2 and 5. Do not treat these package numbers as interchangeable. Ask the supplier to confirm the quoted code and every included component.
What comes with product 304 002 000?
Ambu’s current product-page ordering table names three included elements: the Mark IV size Adult resuscitator, two oxygen reservoir bags, and an Ambu silicone face mask size 5. The size 5 mask is part of this code’s stated kit configuration; it is not evidence that this one mask size is suitable for every intended user or patient. Clinical staff should determine which device and mask configuration is required under their protocol.
Check the final quote against the exact code, particularly if the facility needs a second mask size, additional oxygen supply tubing, spare patient valves, a pressure gauge, a PEEP valve, or other accessories. Ambu lists components and compatible accessory families separately. A part appearing on the manufacturer’s spare-parts page does not mean it is included with 304 002 000. Request separate line items and exact part references for any additional components and have the supplier confirm their compatibility with the Mark IV Adult.
The current Ambu page lists 304 002 000 as a model option, while the manufacturer catalogue also specifies its ordering description. Packaging quantities, market availability, regional product revisions and what a local supplier can obtain must be confirmed in the quotation. Do not rely on older catalogue screenshots or third-party listings as proof of the current contents of a Nigerian offer.
How should I interpret the Mark IV Adult specifications?
Ambu’s Mark IV datasheet lists an approximate resuscitator volume of 1,365 ml for the Adult size. It reports a delivered volume of 600 ml when operated with one hand and 900 ml with two hands under the manufacturer’s stated test conditions. These are technical figures for the product, not a recommendation for a patient and not a promise that the same volume will be delivered in every situation. The results depend on the test method and conditions; real-world use is controlled by trained clinicians and applicable clinical protocols.
The datasheet identifies a patient connector with an outside 22 mm male and inside 15 mm female connection under EN ISO 5356-1, and an expiratory connector for PEEP-valve attachment with a 30 mm male connection. It also lists an oxygen inlet connector according to EN ISO 13544-2. These connector dimensions and standards help biomedical and procurement staff check equipment interfaces, but they do not verify that an arbitrary mask, oxygen supply tube, PEEP valve or accessory is suitable. Confirm exact mating parts and the intended use with the manuals for both devices.
The Mark IV Adult datasheet lists an approximate weight of 415 g without the oxygen reservoir and mask, and approximate dimensions of 270 by 130 mm. These measurements can help with storage-space and emergency-kit planning. Confirm any local storage, transport, cleaning and readiness procedures with the responsible department; this guide does not set a clinical deployment standard.
Which patient range and configuration should a facility request?
The manufacturer identifies the Mark IV Adult for patients over 15 kg. The Mark IV Baby is a separate model size and has its own stated patient range and features, including a pressure-limiting valve. Do not select the Adult model for an individual based only on a product listing or use the Baby model’s pressure-limiting features as if they apply to the Adult model. Patient selection and equipment configuration require qualified clinical judgment and the appropriate manufacturer documentation.
When purchasing for multiple departments, ask each service to confirm the exact model and accessory configuration it requires. A facility may need distinct resuscitator sizes, masks, oxygen reservoir components or accessories for its approved use. List each approved product code separately in the request so the quotation does not collapse two different kits into a generic “Ambu bag.” If the local plan includes additional accessories, request the part numbers and compatibility evidence as separate quote lines.
Ambu also describes the Mark IV as MR Conditional. For any MRI-area use, confirm the exact configuration and restrictions in the current manufacturer instructions and the facility’s MR safety process. Do not infer unrestricted MRI safety, assume accessories have the same MR status, or rely on a general product-family label to approve a particular setup.
How do reuse and reprocessing affect procurement in Nigeria?
Ambu states that the Mark IV resuscitator can be reprocessed up to 30 times. The oxygen reservoir bag has a separate limit of 15 sterilisation cycles, and the oxygen reservoir tube has separate manual-cleaning and disinfection instructions. Those limits differ by component, so the facility needs a way to track cycles for the resuscitator and reservoir bags independently. Do not treat “30 times” as a single cycle limit for every part in the set.
The product page describes the Mark IV as suitable for sterilisation at 134 °C, with the listed exceptions and separate instructions for the reservoir tube. Before ordering a reusable device, have the facility’s infection-prevention, clinical engineering and reprocessing teams check the current IFU against their equipment and validated workflow. Confirm the exact components included, compatible cleaning and sterilisation equipment, cycle records, inspection criteria, replacement parts and retirement process. Do not infer that all components can be autoclaved or processed in the same way.
For Nigerian procurement, include any required manufacturer documentation, instructions for use, batch or lot information, language requirements, receiving documentation, and training or reprocessing questions in the quote request. Whether particular import, registration or facility documentation is required depends on the transaction and applicable local rules; Franance should confirm what documents it can provide for the specific offer. This page makes no claim that the product is registered, in stock or locally supported.
What should I check about accessories and compatibility?
The exact 304 002 000 package is described with two oxygen reservoir bags and a size 5 silicone mask. If a facility needs other mask sizes or a different reservoir arrangement, name the requested configuration rather than assuming the included components can be swapped without review. Ambu’s manuals and accessory listings should be checked for the intended combination. A connection that physically fits is not by itself proof of functional suitability or approval for the planned clinical use.
The datasheet gives the Mark IV patient and expiratory connector dimensions and the oxygen-inlet standard. Share the connected device or accessory make, model and reference with the quotation team. This helps check mask, PEEP valve, oxygen tubing or other accessory requirements against product documentation. Ask the quote to distinguish manufacturer-specified accessories from third-party items and to disclose any proposed substitution for approval.
Ambu warns that adding accessories may affect inspiratory or expiratory resistance. Its instructions also contain operating warnings and require trained users to follow the IFU. For that reason, do not add filters, valves, tubing or adapters based solely on a generic compatibility claim. Have clinical engineering and the responsible clinical team confirm the exact accessory combination for the intended setup.
What should I include in a Mark IV Adult quotation request?
A complete request can include:
- Exact product: Ambu Mark IV Adult, 304 002 000.
- Required unit quantity and delivery city/state in Nigeria.
- Confirmation that the quote includes two reservoir bags and one size 5 Ambu silicone face mask.
- Any additional mask sizes, oxygen tubing, spare parts, PEEP valves, manometers or accessories as separate requested line items.
- Facility requirements for IFU, datasheet, batch/lot, reprocessing-cycle tracking and receipt documentation.
- Intended connected devices or accessory references where compatibility needs review.
- Any minimum remaining shelf life, delivery, quote-validity or payment requirements.
Ask Franance to state the exact model and configuration being offered, confirm availability and delivery terms for the destination, identify substitutions explicitly, and provide written commercial conditions. Do not accept a generic “adult resuscitator” description where the approved requirement is 304 002 000. If a different configuration is proposed, have the clinical and procurement teams compare the included masks, reservoirs and accessories before accepting it.
Frequently asked questions about Ambu Mark IV Adult 304 002 000
### Is 304 002 000 the adult or Baby Mark IV?
It is the Mark IV size Adult configuration. Ambu identifies the Baby model under separate references beginning with 299; product 304 002 000 is listed for the Adult size.
### What exactly is listed in the 304 002 000 configuration?
Ambu lists the adult resuscitator, two oxygen reservoir bags and one size 5 Ambu silicone face mask. Confirm that the written quotation matches this configuration and lists any extras separately.
### What patient weight is the Adult model specified for?
Ambu’s datasheet states the Adult size is suitable for patients over 15 kg. This is manufacturer information, not patient-specific medical advice. Qualified healthcare staff must determine the appropriate device and use.
### Does 304 002 000 include a Baby-size pressure-limiting valve?
The pressure-limiting valve is described for the Mark IV Baby model. Do not assume this feature applies to the adult configuration. Review the applicable product datasheet and IFU.
### How many times can the set be reprocessed?
Ambu lists up to 30 reprocessing cycles for the resuscitator, while the oxygen reservoir bag is limited to 15 sterilisation cycles. The reservoir tube has its own manual cleaning and disinfection instructions. Follow the current IFU component by component.
### Can the Mark IV Adult be used near MRI equipment?
Ambu identifies the Mark IV as MR Conditional. Confirm the exact conditions and configuration in the current IFU and obtain approval through the facility’s MR safety process before use in an MRI environment.
### Can I buy the product online from Franance?
No. Submit a quotation request through Franance. The team follows up by phone or email to confirm the request and commercial terms; the page does not offer online payment or checkout.
Sources and product limitations
This guide is based on Ambu’s Mark IV Reusable Resuscitator product page, the current Mark IV datasheet V09 (2025/09), the Mark IV IFU V06 (2024/02), and Ambu’s anaesthesia catalogue. The Ambu page was reviewed 20 October 2026 and lists the above datasheet and IFU revisions.
All product-performance figures here are manufacturer specifications under stated test conditions, not instructions for patient care or a guaranteed outcome. Follow current manufacturer documentation and trained clinical procedures. Confirm the offered product, accessory compatibility, local documentation and commercial terms. No Nigerian registration, stock, price, lead time, warranty, distributor status, delivery timing or local service entitlement is claimed.