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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, 200" 22/22mm Expandable, Parallel WYE, GSE, Clear, 3L Latex Free Bag, B/V Filter, 1.5' x .050", M/M GSL FDA UDI
Model / Reference
9363 FDA UDI
Description
Anesthesia Circuit, Adult, 200" 22/22mm Expandable, Parallel WYE, GSE, Clear, 3L Latex Free Bag, B/V Filter, 1.5' x .050", M/M GSL FDA UDI

Identifiers

Primary DI / UDI-DI
00709078006104 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

Yes

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 f704207a-1df7-4440-81bd-5f0b9d5d72a0 33 fields · synced May 29, 2026