Anesthesia Coaxial Circuit

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: Anesthesia Coaxial Circuit FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: Coaxial Circuit, 82", GSE, Scavenger Elbow FDA UDI
Model / Reference: 7-6800 FDA UDI
Description: Coaxial Circuit, 82", GSE, Scavenger Elbow FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078009969 FDA UDI
FDA Product Code: OFP FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 868.5240 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Anaesthesia breathing circuit, single-use

Anesthesia Coaxial Circuit by Westmed, Inc. — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Westmed, Inc.

Sources (1)

FDA UDI dfe8f4ab-946f-469a-865e-ae9006286a61 33 fields · synced Jun 8, 2026