eudamed_udi Primary ID: D-023301-9263-327-358D4

kami ITE V50 (UDI D-023301-9263-327-358D4)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The kami ITE V50 (Model/Catalog Number: 023301-9263-327-358) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Y2145060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 023301-9263-327-358
Product Code / EMDN: Y2145060201
Device Name: Hearing aid
Database Sync Date: 2026-08-09 16:29:00

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 kami ITE V50?

The registered manufacturer of record for kami ITE V50 is audifon GmbH & Co. KG.

What is the Primary UDI-DI identifier for kami ITE V50?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-023301-9263-327-358D4.

What classification code is assigned to this device?

This device is registered under product classification code Y2145060201.

Similar Classification Devices (Y2145060201)

Other Devices by audifon GmbH & Co. KG

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