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Anesthesia Breathing System

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Anesthesia Breathing System FDA UDI
Generic Name
Breathing circuit bag, single-use FDA UDI
Device Name
Disposable Anesthesia Breathing System, 1/2L Latex Free Bag, Bleed Tail Valve FDA UDI
Model / Reference
9584 FDA UDI
Description
Disposable Anesthesia Breathing System, 1/2L Latex Free Bag, Bleed Tail Valve FDA UDI

Identifiers

Primary DI / UDI-DI
00709078004315 FDA UDI
FDA Product Code
BTC FDA UDI
GMDN Term
Breathing circuit bag, single-use 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

Anesthesia Breathing System 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 554b068f-d7aa-4a6b-a4b2-30990b073cc3 34 fields · synced Jun 8, 2026