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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Wireless HA receivers — 11 UDI-DI variants, MDR (Phonak AG)

MD Atlas
Phonak AG

Data from EUDAMED, last updated May 23, 2026

Wireless HA receivers

07612904WRASPQ

11 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Phonak AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 07612904WRASPQ
Device name: Wireless HA receivers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: Phonak AG
SRN: CH-MF-000015960
Country: Switzerland
Email: CH-PH-OPS-RA@sonova.com

Authorised representative

Name: Sonova Deutschland GmbH
SRN: DE-AR-000006322
Country: Germany
Phone: +49 711 51070 0

Variants by status

UDI-DI variants

11 UDI-DI variants

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Applied filters

basicUdiUlid01JZ2E9NSD1DZW5XWS52Y4XR38

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

052-3235-D02XN07612904289899
052-3235-D02Q307612904280254
052-3235-D02P407612904280193
052-3235-D02Q107612904280230
052-3235-D02XP 07612904289905
052-3235-D02P907612904280223
052-3235-D02P1 07612904279371
052-3235-D02P607612904280209
052-3235-D02P807612904280216
052-3113-X02P5 07612904391738
052-3488-X02 07613389188028