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Adult Expandable Circuit

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
Adult Expandable Circuit FDA UDI
Generic Name
Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name
144` Adult Expandable Circuit, Mini HMEF, Flex Extender FDA UDI
Model / Reference
9356 FDA UDI
Description
144` Adult Expandable Circuit, Mini HMEF, Flex Extender FDA UDI

Identifiers

Primary DI / UDI-DI
00709078002533 FDA UDI
FDA Product Code
OFP FDA UDI
CAH FDA UDI
GMDN Term
Heat/moisture exchanger/microbial medical gas filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
868.5260 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: Anaesthesia breathing circuit, single-useHeat/moisture exchanger/microbial medical gas filter

Adult Expandable Circuit by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 0b73f410-5add-44db-bb0f-34c6182ce817 33 fields · synced Jun 8, 2026