F&P Neopuff

Neopuff™ Infant T-Piece Resuscitator FR

Registry build 21.09.26
3manufacturers in China registered for this device type
2catalogue numbers in this listing
2recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FMT
Manufacturer City Province Registered as Device types
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Amphenol (Changzhou) Connector Systems Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57

Record

Regulatory record for F&P Neopuff
Listed by Fisher & Paykel Healthcare, Ltd., New Zealand
FDA product code FMT
Device type Warmer, Infant Radiant
Device class Class 2
Regulation 21 CFR 880.5130
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
510(k) K971695
Record published 2016-09-08
Record revised 2026-03-10 (version 6)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for F&P Neopuff
Catalogue number Size Status
RD900AFU In distribution
RD900AEU In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeRoyal Deroyal Industries, Inc. 37
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 9
AirLife™ AirLife Finland Oy 8
Tarry Probes Tarry Medical Products, Inc. 5
Argyle Cardinal Health 5
Panda Datex-Ohmeda, Inc. 4
AccuTemp Probe Kentec Medical, LLC 3
Ameritus Kentec Medical, LLC 3
AirLife Carefusion Finland 320 Oy 3
Sunflower Warmer, Stand AC120V Atom Medical Corporation 2
Heating Element 540W-104V RPI 2
Sunflower Warmer, Wall Mount AC120V Atom Medical Corporation 2

Showing 12 of 39. All products under Warmer, Infant Radiant

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2014-11-06 Class II Manufacturing material removal Breakage of the nut that secures the heater head in place, which can cause the heater head to become partially detached and swing towards the bassinet. There is the potential that a heater head could contact a patient situated on the bassin Nationwide (U.S.): 661 Infant Warmers and 180 Spare Parts, I 2015-04-27
2006-10-09 Not classified Other This firm has received Product Complaint Reports concerning bending of the pivot plate. The elevator base of the CosyCot Infant Warmer incorporates a pivot plate which forms part of the mechanism allowing the CosyCot to raise and lower in h 273 units in US & 9 in Canada 2012-04-26

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer