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BagEasy

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
BagEasy FDA UDI
Generic Name
Pulmonary resuscitator, manual, single-use FDA UDI
Device Name
Adult BagEasy Resuscitator FDA UDI
Model / Reference
562041 FDA UDI
Description
Adult BagEasy Resuscitator FDA UDI

Identifiers

Primary DI / UDI-DI
00709078620416 FDA UDI
510(k) Number
K934310 FDA UDI
FDA Product Code
BTM FDA UDI
GMDN Term
Pulmonary resuscitator, manual, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5915 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pulmonary resuscitator, manual, single-use

BagEasy by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary resuscitator, manual, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 29ea6f02-9dd9-462c-bd9d-7ab8972c3a84 34 fields · synced May 31, 2026