Circulaire II Aerosol Drug Delivery System

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: Circulaire II Aerosol Drug Delivery System FDA UDI
Generic Name: Heat/moisture exchanger/microbial medical gas filter FDA UDI
Device Name: With extra reservoir bag, with B/V filter, 7' tubing w/threaded nut FDA UDI
Model / Reference: 0329 FDA UDI
Description: With extra reservoir bag, with B/V filter, 7' tubing w/threaded nut FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078000737 FDA UDI
FDA Product Code: CAH FDA UDI
CAF 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
868.5630 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Heat/moisture exchanger/microbial medical gas filter Nebulizing system delivery set, single-use

Circulaire II Aerosol Drug Delivery System by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Westmed, Inc.

Sources (1)

FDA UDI 00360b84-5ff0-437d-bcd8-dc3af2712b68 33 fields · synced Jun 1, 2026