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Breathing Bag

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Breathing Bag FDA UDI
Generic Name
Breathing circuit bag, reusable FDA UDI
Device Name
Breathing Bag, 1/2L, Not Made With Latex FDA UDI
Model / Reference
6395 FDA UDI
Description
Breathing Bag, 1/2L, Not Made With Latex FDA UDI

Identifiers

Primary DI / UDI-DI
00709078008542 FDA UDI
FDA Product Code
BTC FDA UDI
GMDN Term
Breathing circuit bag, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5320 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Breathing Bag by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI cdbb3862-b4f8-4b01-936f-ebc1ddaf5392 34 fields · synced May 30, 2026