72' Adult Uni-Lim™ Coaxial Anesthesia Circuit

FDA UDI

Class II (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name: 72' Adult Uni-Lim™ Coaxial Anesthesia Circuit FDA UDI
Generic Name: Anaesthesia breathing circuit, single-use FDA UDI
Device Name: 72' Adult Uni-Lim™ Coaxial Anesthesia Circuit, GSE, Inline Mini HMEF, 2L/Lf FDA UDI
Model / Reference: 9128 FDA UDI
Description: 72' Adult Uni-Lim™ Coaxial Anesthesia Circuit, GSE, Inline Mini HMEF, 2L/Lf FDA UDI

Identifiers

Primary DI / UDI-DI: 00709078002489 FDA UDI
FDA Product Code: CAH FDA UDI
GMDN Term: Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 868.5260 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

Yes

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: Anaesthesia breathing circuit, single-use

72' Adult Uni-Lim™ Coaxial Anesthesia Circuit by Westmed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Vital Signs™ — Airlife, Inc. · Class II
HUDSON RCI — TELEFLEX INCORPORATED · Class I
Vital Signs™ — Airlife, Inc. · Class I
UNIVERSAL FLEX2®BREATHING CIRCUIT & PACK KIT — KING SYSTEMS CORPORATION. · Class I
Vital Signs™ — Airlife, Inc. · Class I
Portex — ICU MEDICAL, INC. · Class I
UNIVERSAL FLEX2® — KING SYSTEMS CORPORATION. · Class I
PEDIATRIC ULTRA FLEX® — KING SYSTEMS CORPORATION. · Class I

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Westmed, Inc.

Sources (1)

FDA UDI 99b6f2a7-f394-47a9-94d8-2146172f53d0 33 fields · synced May 30, 2026