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Disposable Circuit

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Disposable Circuit FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
Circuit, Disposable, 22mm, Non-Heated Dual Limb w/ BV filter FDA UDI
Model / Reference
8205 FDA UDI
Description
Circuit, Disposable, 22mm, Non-Heated Dual Limb w/ BV filter FDA UDI

Identifiers

Primary DI / UDI-DI
00709078008672 FDA UDI
510(k) Number
K922492 FDA UDI
FDA Product Code
CAH FDA UDI
CAI FDA UDI
GMDN Term
Heat/moisture exchanger/microbial medical gas filter 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Heat/moisture exchanger/microbial medical gas filter

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

Similar devices

Also classified as Heat/moisture exchanger/microbial medical gas filter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 134e7d19-d273-4df8-be16-aabbb33648f7 34 fields · synced Jun 1, 2026