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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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Clue — 2 UDI-DI variants, MDR (Biowink GmbH)

MD Atlas
Biowink GmbH

Data from EUDAMED, last updated May 23, 2026

Clue

426074984ClueND

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: Biowink GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426074984ClueND
Device name: Clue
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: Jul 27, 2023

Manufacturer & authorised representative

Manufacturer

Name: Biowink GmbH
SRN: DE-MF-000030007
Country: Germany
Email: giulia.paggiola.ext@helloclue.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H6BKDTB9G6GN3RCVNZZYV7MN

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

Clue (Android)04260749840046
Clue (iOS)04260749840039