gudid Primary ID: 00-422

AincA (UDI 00-422)

Manufactured by ANESTHESIA ASSOCIATES, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AincA (Model/Catalog Number: 00-422) is a medical device manufactured by ANESTHESIA ASSOCIATES, INC.. This product is indexed under FDA Product Code / Category Classification CBP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 00-422
Product Code / EMDN: CBP
Device Name: Valve, Non-Rebreathing, 90, Adjustable Pop-Off, 7/8" x 22mmM/15mmF, w/Thumb Control, Chrome Brass
Database Sync Date: 2026-08-09 09:16:44

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 AincA?

The registered manufacturer of record for AincA is ANESTHESIA ASSOCIATES, INC..

What is the Primary UDI-DI identifier for AincA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00-422.

What classification code is assigned to this device?

This device is registered under product classification code CBP.

Similar Classification Devices (CBP)

Other Devices by ANESTHESIA ASSOCIATES, INC.

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