GUDIDData
eudamed_udi Primary ID: 04038953889430

HA OZ 20 RIC 312 G6 BG (UDI 04038953889430)

Manufactured by AS AUDIO-SERVICE GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HA OZ 20 RIC 312 G6 BG - Primary ID 04038953889430

Device Regulatory Overview

The HA OZ 20 RIC 312 G6 BG (Model/Catalog Number: 10992014) is a medical device manufactured by AS AUDIO-SERVICE GmbH. This product is indexed under FDA Product Code / Category Classification Y2145060102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10992014
Product Code / EMDN
Y2145060102
Device Name
RIC
Database Sync Date
2026-08-09 16:46:56

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 HA OZ 20 RIC 312 G6 BG?

The registered manufacturer of record for HA OZ 20 RIC 312 G6 BG is AS AUDIO-SERVICE GmbH.

What is the Primary UDI-DI identifier for HA OZ 20 RIC 312 G6 BG?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04038953889430.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060102.

Programmatic Export

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

JSON API Endpoint