← Back to catalogue

Disposable Anesthesia Circuits

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Disposable Anesthesia Circuits FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
Anesthesia Circuit, Adult, 48", GSE w/CAP, Parallel WYE, B/V Filter, 3L latex free breathing bag FDA UDI
Model / Reference
ca3103 FDA UDI
Description
Anesthesia Circuit, Adult, 48", GSE w/CAP, Parallel WYE, B/V Filter, 3L latex free breathing bag FDA UDI

Identifiers

Primary DI / UDI-DI
00709078011283 FDA UDI
510(k) Number
K922492 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
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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

Cleared under the same submission

K922492 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 38b4df69-4fc5-4048-8735-5180af423913 35 fields · synced May 31, 2026