gudid Primary ID: 9187

120" Anesthesia Breathing Circuit (UDI 9187)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 120" Anesthesia Breathing Circuit (Model/Catalog Number: 9187) 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: 9187
Product Code / EMDN: CAH
Device Name: 120" Anesthesia Breathing Circuit, B/V Filter, GSE 10' x .060 ID M/M GSL, In-line Mini HMEF, Parallel WYE w/Temperature Port and GSP, 3L not made made with latex bag, 900 large adult mask
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 120" Anesthesia Breathing Circuit?

The registered manufacturer of record for 120" Anesthesia Breathing Circuit is WESTMED, INC..

What is the Primary UDI-DI identifier for 120" Anesthesia Breathing Circuit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9187.

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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