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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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Clôppe — 10 UDI-DI variants, MDR (DocCheck Steam GmbH)

MD Atlas
DocCheck Steam GmbH

Data from EUDAMED, last updated May 23, 2026

Clôppe

426256008101649BC

10 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: DocCheck Steam GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426256008101649BC
Device name: Clôppe
Device model: Clôppe
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: DocCheck Steam GmbH
SRN: DE-MF-000050235
Country: Germany
Email: lab@doccheck.com

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KBQ2MCAEEZ3GBE1E4EBCVNS2

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

101649.1 04262560080069
101649.4 04262560080045
101649.3 04262560080052
101649.5 04262560080038
101649.2 04262560080007
101649.0 04262560080021
102956.1 04262560080090
102956.0 04262560080106
101650.0 04262560080076
101650.2 04262560080083