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Anesthesia Circuit

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Anesthesia Circuit FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Anesthesia Circuit, Adult, UNI-LIM, 72" GSE, 10' x .050 ID M/M GSE, 3L Latex Free Bag, B/V Filter FDA UDI
Model / Reference
9670 FDA UDI
Description
Anesthesia Circuit, Adult, UNI-LIM, 72" GSE, 10' x .050 ID M/M GSE, 3L Latex Free Bag, B/V Filter FDA UDI

Identifiers

Primary DI / UDI-DI
00709078006326 FDA UDI
FDA Product Code
CAH FDA UDI
OFP FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 FDA UDI
868.5240 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia breathing circuit, single-use

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

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 75323615-ebb8-4fe9-86d6-28488af0ce2e 33 fields · synced Jun 8, 2026