The BAG Manometer

The BAG Manometer is a non-sterile single use accessory for displaying the airway pressure use with Laerdal The BAG resuscitator. It may be used for single-patient multiple use when kept…

Registry build 21.09.26

The BAG Manometer is a non-sterile single use accessory for displaying the airway pressure use with Laerdal The BAG resuscitator. It may be used for single-patient multiple use when kept free from contamination.

7manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Guangdong (3), Fujian (2), Jiangsu (1). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CAP
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Flexicare Medical (Dongguan) Ltd. Dongguan Guangdong Contract manufacturer 48
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Ambu Limited Xiang Yu F.T.Z., Xiamen Fujian Contract manufacturer 11
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
GaleMed (Xiamen) Co., Ltd. Xiamen Fujian Contract manufacturer 33
Laerdal Medical (Suzhou) Co., Ltd. 215009 Suzhou Jiangsu Province Repacker / relabeller 12

Record

Regulatory record for The BAG Manometer
Listed by Laerdal Medical Corp., United States
FDA product code CAP
Device type Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Device class Class 2
Regulation 21 CFR 868.2600
510(k) K251631
Record published 2026-01-14

Specifications

Specifications
MRI safety MR Conditional
Single use Yes
Prescription Prescription only
Latex Labelled latex-free
Label carries lot or batch number
Storage Storage environment temperature -40 to 70 °C
Packaging Carton of 12

Catalogue Numbers

Catalogue numbers for The BAG Manometer
Catalogue number Size Status
8470401 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
AincA® Anesthesia Associates, Inc. 24
Manometer Mercury Medical Enterprises, LLC 18
Jaeger Jaeger Medical GmbH 9
Vyaire Jaeger Medical GmbH 8
Medline Industries, Inc. Medline Industries, Inc. 6
Jitto Galemed Corp. 6
Napa DRW Medical 5
Micro Medical Jaeger Medical GmbH 4
Monitor, Airway Pressure (Includes Gauge And/Or Alarm) GE Healthcare Finland OY 4
Monitor, Airway Pressure (Includes Gauge And/Or Alarm) Galemed Corp. 3
Resuscitator Manometer POP OFF 60cmH2O(PC) Besmed Health Business Corporation 2
Cuff Pressure Monitor Assembly Instrumentation Industries, Incorporated 2

Showing 12 of 44. All products under Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

PMA Approvals

A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.

FDA premarket approvals naming this product code
PMA number Decision Trade name Approved to
N83074 1985-03-22 NON-ABSORBABLE BLACK SILK SUTURE Look, Inc.

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