Who else makes this device?

Name: Smart BAG MO
Brand: Smart BAG MO

Anesthesiology › TherapeuticVentilator, Emergency, Powered (Resuscitator)

Smart BAG MO

The SMART BAG MO Manual Resuscitator is Bag Valve Mask Resuscitator comprising a self inflating bag, a one way valve and a face mask designed to supply accurate controlled ventilation to a…

Registry build 21.09.26

The SMART BAG MO Manual Resuscitator is Bag Valve Mask Resuscitator comprising a self inflating bag, a one way valve and a face mask designed to supply accurate controlled ventilation to a non-breathing patient by the compression of the bag portion of the device by the operator. Similar in all respects to the conventional BVMs, the SMART BAG MO offers accurate controlled ventilation that significantly reduces the risk of gastric insufflation. The patient’s airway pressure is maintained at an optimally low level due to the SMART® technology in the bag that responds to both the rescuer’s squeeze of the bag and the patient’s own respiratory condition. It is designed for use in various clinical settings to provide respiratory support to the respiratory distressed or non-breathing Child patient.

4manufacturers in China registered for this device type

1catalogue number

5510(k) clearances naming this product code

3recalls on this code

Who Else Makes It

Concentrated in Guangdong (3), Fujian (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 BTL
Manufacturer	City	Province	Registered as	Device types
GaleMed (Xiamen) Co., Ltd.	Xiamen	Fujian	Contract manufacturer	33
Sunmed AP, Ltd.	Zhuhai	Guangdong	Contract manufacturer	18
Sunmed AP, Ltd., Warehouse NO. 2	Zhuhai	Guangdong	Contract manufacturer	16
Dongguan Plastiflex Hose Technology Ltd	Dongguan	Guangdong	Contract manufacturer	3

Record

Regulatory record for Smart BAG MO
Listed by	O-TWO Medical Technologies, Inc., Canada
FDA product code	BTL
Device type	Ventilator, Emergency, Powered (Resuscitator)
Device class	Class 2
Regulation	21 CFR 868.5925
Establishment	Specification developer, Repacker / relabeller, Manufacturer, Exporter
510(k)	K021328
Record published	2015-10-23
Record revised	2018-07-06 (version 3)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Single use	Yes
Prescription	Prescription only
Label carries	lot or batch number, expiry date
Storage	Storage environment temperature -18 to 50 °C
Packaging	Corrugated carton of 12

Catalogue Numbers

Catalogue numbers for Smart BAG MO
Catalogue number	Size	Status
01BM3210-MO		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Life Support Products	Allied Medical LLC	50
Neo-Tee T-Piece Resuscitator	Mercury Medical Enterprises, LLC	45
Pneupac	ICU Medical, Inc	38
Allied Medical LLC	Allied Medical LLC	19
Fisher & Paykel Healthcare	Fisher & Paykel Healthcare, Ltd.	18
AincA	Anesthesia Associates, Inc.	17
Neo-Tee T-Piece Resuscitator Circuit	Mercury Medical Enterprises, LLC	12
Life Support Products (LSP)	Allied Medical LLC	12
Moves	Thornhill Research Inc.	11
Ventlab	Ventlab, LLC	7
Resusa-Tee T-Piece Resuscitator	Mercury Medical Enterprises, LLC	7
Curaplex	Bound Tree Medical, LLC	5

Showing 12 of 70. All products under Ventilator, Emergency, Powered (Resuscitator)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K141595	2015-03-16
K093862	2010-05-06
K081330	2009-03-06
K051469	2005-09-28
K051889	2005-08-30

Recalls

3 of these are Class I. Class I is the FDA’s most serious grade: a reasonable probability of serious injury or death. 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
2019-02-12	Class I	Process control	There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main boa	119	2023-06-29
2019-02-12	Class I	Process control	There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main boa	136	2023-06-29
2019-02-12	Class I	Process control	There is a potential for the unit to catch fire due to one of the screen retaining screws being incorrectly inserted. Due to this improper screw insertion the screw sat higher than normal allowing it to contact the underside of the main boa	632	2023-06-29

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.