gudid Primary ID: 9153A

Uni-Lim Coaxial Circuit (UDI 9153A)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Uni-Lim Coaxial Circuit (Model/Catalog Number: 9153A) is a medical device manufactured by WESTMED, INC.. This product is indexed under FDA Product Code / Category Classification CAH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 9153A
Product Code / EMDN: CAH
Device Name: Anesthesia Circuit, Adult, Uni-Lim, 60", Co-Axial, GSE, 3L Not Made With Latex Bag, 10' x .050' ID M/M GSL, 900 Series Large Adult Mask, HEPA Filter, In-Line Mini HMEF, Hose Clip
Database Sync Date: 2026-08-09 09:04:13

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Uni-Lim Coaxial Circuit?

The registered manufacturer of record for Uni-Lim Coaxial Circuit is WESTMED, INC..

What is the Primary UDI-DI identifier for Uni-Lim Coaxial Circuit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9153A.

What classification code is assigned to this device?

This device is registered under product classification code CAH.

Similar Classification Devices (CAH)

Other Devices by WESTMED, INC.

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