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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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Verschlusskappen — 4 UDI-DI variants, MDR

MD Atlas
Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH

Data from EUDAMED, last updated May 23, 2026

Verschlusskappen

426074129KappenY7

4 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: Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426074129KappenY7
Device name: Verschlusskappen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: Theodor Labarre Werkstätte für silb. chirurg. Instrumente GmbH
SRN: DE-MF-000011889
Country: Germany
Email: th@labarre-gmbh.de
Phone: +49 7161 914400

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01G6E1VMPA4MDA4KQ55P2C40NP

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

1726D04260741290320
1988904260741290313
1981004260741290306
1068204260741290290