gudid Primary ID: 9698

Adult Expandable Circuit (UDI 9698)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Adult Expandable Circuit (Model/Catalog Number: 9698) 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: 9698
Product Code / EMDN: CAH
Device Name: Anesthesia Circuit, Adult, 108" Expandable, Swivel Wye w/ GSP, 3 LF Breathing Bag
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 Adult Expandable Circuit?

The registered manufacturer of record for Adult Expandable Circuit is WESTMED, INC..

What is the Primary UDI-DI identifier for Adult Expandable Circuit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9698.

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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