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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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Audio Personal Amplifier Device — 2 UDI-DI variants, MDR

MD Atlas
Bellman & Symfon Group AB

Data from EUDAMED, last updated May 31, 2026

Audio Personal Amplifier Device

73316460106N

2 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: Bellman & Symfon Group AB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 73316460106N
Device name: —
Device model: Audio Personal Amplifier Device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Bellman & Symfon Group AB
SRN: SE-MF-000046749
Country: Sweden
Email: info@bellman.com
Phone: +4631682820

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JV9YNXXRTC4A6XS6KH7N7T8K

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

Maxi Personal Amplifier07331646003487
Mino Personal Amplifier07331646003500