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Bacterial/Viral Respiratory Filter

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Bacterial/Viral Respiratory Filter FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Model / Reference
0242 FDA UDI

Identifiers

Primary DI / UDI-DI
00709078000713 FDA UDI
510(k) Number
K922492 FDA UDI
FDA Product Code
CAH 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
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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Bacterial/Viral Respiratory Filter 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

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 84d2d424-26b2-4ab4-ae49-08c0ffc0323a 34 fields · synced Jun 8, 2026