eudamed_udi Primary ID: D-023172-9044-313-1720HL

rega S (UDI D-023172-9044-313-1720HL)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The rega S (Model/Catalog Number: 023172-9044-313-1720) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Y2145060101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 023172-9044-313-1720
Product Code / EMDN: Y2145060101
Device Name: Hearing aid
Database Sync Date: 2026-08-09 16:30:27

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 rega S?

The registered manufacturer of record for rega S is audifon GmbH & Co. KG.

What is the Primary UDI-DI identifier for rega S?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-023172-9044-313-1720HL.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060101.

Similar Classification Devices (Y2145060101)

Other Devices by audifon GmbH & Co. KG

Programmatic Export

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

JSON API Endpoint