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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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Softband — 76 UDI-DI variants, MDR (Oticon Medical AB)

MD Atlas
Oticon Medical AB

Data from EUDAMED, last updated May 30, 2026

Softband

57121491000386

76 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: Oticon Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57121491000386
Device name: Softband
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Oticon Medical AB
SRN: SE-MF-000000724
Country: Sweden
Email: kije@oticonmedical.com

Variants by status

UDI-DI variants

76 UDI-DI variants

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Applied filters

basicUdiUlid01G0H6RA0P5YN6R6W88ZSNFP52

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

No registered UDI-DI variants for this device family.