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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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Tŭlip — 5 UDI-DI variants, MDR (DocCheck Steam GmbH)

MD Atlas
DocCheck Steam GmbH

Data from EUDAMED, last updated May 23, 2026

Tŭlip

426256008102527B4

5 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: 426256008102527B4
Device name: Tŭlip
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 8, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01KBZ6CKS5H7PA0G67WHTVAF4G

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

102527.2 04262560080113
102527.4 04262560080120
102527.5 04262560080137
102703.1 04262560080144
102703.2 04262560080533