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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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Klebetuch — 6 UDI-DI variants, MDR

MD Atlas
Udo Heisig GmbH The Disposables Company

Data from EUDAMED, last updated May 23, 2026

Klebetuch

42518062006L8

6 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: Udo Heisig GmbH The Disposables Company

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518062006L8
Device name: Klebetuch
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Udo Heisig GmbH The Disposables Company
SRN: DE-MF-000009334
Country: Germany
Email: info@heisig.de
Phone: 0894623920

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVKYFMC3SPGJR6ZDY4Y3YTYT

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

3705704251806200910
3704904251806202587
3706004251806203522
3705404251806200903
3705904251806200927
3914104251806201115