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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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Frottee-Stumpfstrumpf — 2 UDI-DI variants, MDR

MD Atlas
ORTHO-REHA Neuhof GmbH

Data from EUDAMED, last updated May 23, 2026

Frottee-Stumpfstrumpf

42518119203D27MN

2 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: ORTHO-REHA Neuhof GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518119203D27MN
Device name: Frottee-Stumpfstrumpf
Device model: Frottee-Stumpfstrumpf
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: ORTHO-REHA Neuhof GmbH
SRN: DE-MF-000008438
Country: Germany
Email: raphael.stecher@ortho-reha-neuhof.de

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JT0X1EQDRPN2YRZPYN2XX04B

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

203B04251811901338
203B04251811901345