Buy Bag Valve Mask (BVM) Resuscitators in Nigeria.

Where can I buy BVM resuscitators in Nigeria?

Use the bag valve mask resuscitator category to compare the six catalogue records and their filtered model listings. These are manual resuscitator product records. They are not mechanical ventilators, oxygen cylinders, suction devices, or complete emergency-room packages. If the purchasing plan requires any of those items, name them separately in the enquiry and ask the quotation to show each line and included accessory.

Send Franance your exact manufacturer and item number, quantity, required population-size configuration as defined by your organization, intended reusable or single-patient-use procurement policy, delivery address, and documentation requirements. If the products are for multiple wards, vehicles or facility sites, separate the quantities and destinations so the offer can specify the right pack configuration and delivery terms. Franance can then follow up by phone or email with questions tied to the quote order.

Which BVM models does Franance list?

The six current assignments are Ambu SPUR II Adult, product 325 002 000, Ambu SPUR II Paediatric, product 330 003 000, and the Ambu Mark IV Adult, product 304 002 000. Laerdal records are the LSR Paediatric Standard Child with Mask, item 86005233, LSR Adult Complete, item 87005133, and The BAG Adult with size 5 mask, item 84735040.

The model numbers matter. Ambu describes SPUR II as single-patient use and Mark IV as reusable. Laerdal describes its silicone resuscitator (LSR) as reusable, while The BAG is a single-use line. Within those families, size, mask, reservoir and other included items vary by item code. Check the exact item and pack details in the written quote rather than assuming two records with the same general device type have the same contents.

How do I choose between single-use and reusable BVMs?

Use the procurement policy set by your facility’s clinical, infection-prevention, biomedical engineering and procurement leads. A single-use device and a reusable device carry different stock, reprocessing, storage and lifecycle requirements. The manufacturer identifies the Ambu SPUR II and Laerdal The BAG as single-use products; Ambu Mark IV and Laerdal LSR are reusable product families. These classifications are not a recommendation for one policy over another and do not replace the manufacturer instructions for use or the facility’s approved process.

For a single-use model, specify the exact packaged configuration, expiry or shelf-life information required by your purchasing policy, storage conditions, quantity basis and disposal expectations. For a reusable model, request the current manufacturer reprocessing instructions, compatible sterilization or disinfection method, component replacement criteria, inspection documentation and any cycle limits applicable to each component. A reusable designation alone does not tell you the reprocessing infrastructure, cost or turnaround time your site needs. Ask the supplier to identify replacement parts and any components that have different service lives or reprocessing limits.

How should I compare adult and paediatric BVM configurations?

Select a catalogue item only after the responsible clinical team has defined the population and product-size specification for the facility. This guide does not recommend patient sizing or clinical selection. Product family labels such as adult, paediatric, child, infant or neonatal are not enough to identify the exact supplied set. Confirm the model code, manufacturer’s intended population range in the current instructions, bag configuration, mask size, reservoir, oxygen tubing, pressure-limiting component and other accessories for the offered item.

The catalogue’s Ambu paediatric record is SPUR II product 330 003 000; Ambu’s product page lists this as a paediatric configuration with an infant mask. The Laerdal paediatric record is an LSR Standard Child with mask, item 86005233. The adult listings are likewise different: SPUR II adult 325 002 000, reusable Mark IV adult 304 002 000, LSR Adult Complete 87005133 and The BAG Adult with size 5 mask 84735040. Ask for each model’s current item-level manufacturer documentation, not a family brochure alone, and have the facility verify that the proposed specification matches its own clinical policy.

What is included with each BVM configuration?

Do not assume a BVM listing includes every accessory shown in a manufacturer image. Mask sizes, oxygen reservoir or reservoir tube, oxygen tubing, carrying case, manometer, PEEP valve, filters, spare components and user documentation can vary by model number or purchased option. The Ambu product page identifies product-number-specific SPUR II combinations; for example, 325 002 000 is listed with an adult bag reservoir, oxygen tubing and medium adult mask, while 330 003 000 is listed with reservoir, oxygen tubing and infant mask. The Mark IV 304 002 000 configuration includes a reservoir and mask configuration. Laerdal’s LSR Adult Complete and paediatric Standard Child configurations also differ in masks and included items.

Laerdal item 84735040 appears as a 12-pack in the manufacturer’s catalogue, with the resuscitator, oxygen reservoir, size 5 mask and oxygen tubing described as included. Confirm the quote’s order unit and pack quantity before comparing per-unit prices or entering stock quantities. Packaging and item descriptions can differ between regions or revisions. Ask the written offer to name the full manufacturer description, order code, pack size, mask, reservoir, tubing and every optional accessory included.

What should I check about masks, oxygen connections and accessories?

Ask the supplier to provide the official technical documentation for the exact offered item and its accessories. Confirm mask size and type, patient connector, oxygen inlet and tubing, reservoir, expiratory or accessory connections, and whether a manometer or PEEP valve is part of the ordered set or a separate accessory. If your organization requires particular connectors or accessories, give the exact part reference and ask the supplier to confirm compatibility in writing. Do not infer compatibility from photographs or from the product family name.

If your technical specification cites connectors or accessory standards, include the exact edition and requested evidence in the enquiry. Request the manufacturer’s conformity or technical documents for the specific model and relevant accessories. Any connection to oxygen supply or other equipment should be verified by the hospital’s responsible technical professionals against current instructions. This is procurement information only, not a setup procedure or operating instruction.

What should I request for reusable BVM reprocessing?

For a reusable model, ask for current instructions for use and reprocessing documents that apply to the exact catalogued item. Confirm which components can be cleaned, disinfected or sterilized, the permitted method and parameters, any component-specific cycle limitations, inspection criteria, drying and assembly requirements, storage conditions, replacement parts, and how to document maintenance. Check whether the oxygen reservoir bag, tubing, valve parts, mask and carrying case have the same reprocessing status; do not assume they do.

Ambu’s Mark IV documentation distinguishes the main reusable resuscitator from some reservoir components, and the manufacturer gives separate reprocessing limits for the reservoir bag and reservoir tube. Laerdal provides user information for the LSR family. Use the latest manufacturer documents and your institution’s validated process; the category guide is not a substitute. If the required reprocessing process is unavailable at your site, raise that as a procurement constraint before approving a reusable configuration.

What documents should accompany a BVM quotation?

Request a model-specific product datasheet, current instructions for use, technical specifications, applicable conformity or regulatory documentation, item number and packaging description. For reusable devices, also request the reprocessing instructions, compatible sterilization/disinfection scope, maintenance schedule, component replacement details and any documented reprocessing cycle limits. For single-use models, request shelf-life and storage information relevant to the exact lot or proposed supply, if your policy requires it. If standards or certifications are specified in a tender, ask for the actual product-specific evidence rather than relying on a general manufacturer statement.

The World Health Organization’s medical-device procurement guidance frames technical specifications as tools for tendering, purchasing, implementation, maintenance and training. Apply that approach by defining the required device, accessories, documentation, support and acceptance checks before comparing offers. WHO technical information does not establish Nigerian regulatory status for any product in this catalogue. Have the responsible regulatory and procurement stakeholders verify requirements that apply to the intended import and use.

How much do BVM resuscitators cost in Nigeria?

Franance does not show a confirmed fixed price for these six models. A quote may vary with model and item code, patient-size configuration, reusable or single-use design, mask and reservoir contents, pack size, accessories, quantity, destination and supply terms. Compare quotes on the exact same order unit and included configuration. A 12-pack must not be compared to a single unit as if both quantities were equivalent.

Ask the written quotation to separate unit or pack price, currency, quantity, taxes and applicable charges, quotation validity, delivery, any requested accessories, and any service or warranty terms. For reusable configurations, include the intended replacement parts and reprocessing documentation needed for lifecycle planning. For single-use configurations, ask for the package quantity and expiry information required by your purchasing process. The category listing does not establish price, local stock or availability for any destination in Nigeria.

Can Franance deliver BVM resuscitators to my state or city?

Include the complete facility delivery address, city and state, receiving contact, requested quantity and delivery timing in your enquiry. The product listing does not confirm stock, import eligibility, delivery coverage, dispatch date, taxes or shipping charges for any Nigerian location. Ask Franance to confirm these terms in writing for the exact product and quantity before relying on a timeline.

For multiple hospitals, emergency departments, ambulances or other receiving units, list each destination and requested quantity separately. State any packaging, lot, shelf-life or document requirements your receiving process needs. If you need training, maintenance or reprocessing support, ask whether the proposed supplier can provide it for your location and whether it is included, chargeable or outside the quotation. Do not infer local service availability from the manufacturer’s international product page.

Can I buy BVM resuscitators online from Franance?

No. Franance accepts quote orders, not online payment. Shortlist the exact product and quantity, submit your enquiry, and Franance will follow up by phone or email to clarify the request and provide quotation details. An enquiry is not a confirmed order, payment, stock reservation or delivery commitment.

How do I request a BVM resuscitator quote from Franance?

Choose from the six filtered BVM model listings and include the exact manufacturer, model, item number, configuration, pack size and quantity. Specify the facility city and state, the documentation required, single-use or reusable purchasing policy, any accessories or connector requirements, storage or expiry needs, and the requested delivery timeframe. For reusable models, request the current reprocessing and component-limit documents. For single-use models, confirm the order unit, package contents and shelf-life information required for receipt.

Ask the written offer to state product identity, order unit, exact inclusions and exclusions, price, availability, delivery terms, applicable documentation, and any warranty, training or service scope. Franance can then follow up by phone or email. Request a BVM resuscitator quotation from Franance.

Sources and scope notes

This guide covers the six current Franance catalogue records in the BVM resuscitator category. Manufacturer sources support product-family classification and item-level descriptions only; configurations, package quantities and documents can vary by market or revision. Confirm details for the exact item quoted. This is purchasing guidance, not clinical advice, device-use training, reprocessing instructions, engineering approval or a Nigerian regulatory determination.

- Ambu SPUR II Disposable Resuscitator and Ambu SPUR II instructions for use
- Ambu Mark IV Reusable Resuscitator and Mark IV datasheet
- Laerdal Silicone Resuscitator (LSR) and LSR Adult Complete item 87005133
- Laerdal The BAG item 84735040 and The BAG Adult user guide
- WHO manual resuscitator device record and WHO user guide to technical specifications for medical devices