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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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Manual Stretcher — 3 UDI-DI variants, MDR (Stollenwerk u. Cie. GmbH)

MD Atlas
Stollenwerk u. Cie. GmbH

Data from EUDAMED, last updated May 31, 2026

Manual Stretcher

42518823MS-01DQ

3 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: Stollenwerk u. Cie. GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518823MS-01DQ
Device name: Manual Stretcher
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Stollenwerk u. Cie. GmbH
SRN: DE-MF-000048989
Country: Germany
Email: info@stollenwerk-koeln.de
Phone: +492219684030

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS7DQ7MDA62HDYQCAH44JWAB

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

400204251882300023
4002-104251882300030
300604251882300016