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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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Gravierte Alu-Membransets "Drums" — 11 UDI-DI variants, MDR

MD Atlas
DocCheck Steam GmbH

Data from EUDAMED, last updated May 23, 2026

Gravierte Alu-Membransets "Drums"

426256008103395BJ

11 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: 426256008103395BJ
Device name: Gravierte Alu-Membransets "Drums"
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 11, 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

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KC6B18CRQ205E2RSCZ6Y278V

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

103395.1 04262560080373
103395.304262560080694
103395.2 04262560080380
104361.004262560080656
104495.104262560080724
103435.2 04262560080526
103435.0 04262560080502
103395.0 04262560080366
104361.104262560080663
103435.1 04262560080519
104361.204262560080670