eudamed_udi Primary ID: D-023305-9112-334-358BM

rega CIC (UDI D-023305-9112-334-358BM)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The rega CIC (Model/Catalog Number: 023305-9112-334-358) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Y2145060203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 023305-9112-334-358
Product Code / EMDN: Y2145060203
Device Name: Hearing aid
Database Sync Date: 2026-08-09 16:28:52

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 CIC?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-023305-9112-334-358BM.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060203.

Similar Classification Devices (Y2145060203)

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