gudid Primary ID: 9700

Anesthesia/Breathing Circuits (UDI 9700)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Anesthesia/Breathing Circuits (Model/Catalog Number: 9700) 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: 9700
Product Code / EMDN: CAH
Device Name: 120" Adult 22mm/2mm Expandable Circuit, Parallel WYE, 2() B/V Filters, Mini HEMF W/ CO2 Port, Adult Vent Mask, 2L not made with latex breathing bag, Sterile Yankuer, W/Bulb Tip, 10' x 0.050 M/M GSL, 10' Suction Tubing
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 Anesthesia/Breathing Circuits?

The registered manufacturer of record for Anesthesia/Breathing Circuits is WESTMED, INC..

What is the Primary UDI-DI identifier for Anesthesia/Breathing Circuits?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 9700.

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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