gudid Primary ID: 00-279-CASE

AincA (UDI 00-279-CASE)

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: 00-279-CASE) is a medical device manufactured by ANESTHESIA ASSOCIATES, INC.. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 00-279-CASE
Product Code / EMDN: BZG
Device Name: Case, Black, Carry, With Foam in Lid and Base. For 00-279 Professional Peak Flow Meter.
Database Sync Date: 2026-08-09 09:16:44

Full Regulatory Attributes

🔒 Token Gated

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 00-279-CASE.

What classification code is assigned to this device?

This device is registered under product classification code BZG.

Similar Classification Devices (BZG)

Other Devices by ANESTHESIA ASSOCIATES, INC.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint