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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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Mehrfachkompressen heiß/kalt — 89 UDI-DI variants, MDR

MD Atlas
Schneider Medical GmbH

Data from EUDAMED, last updated May 23, 2026

Mehrfachkompressen heiß/kalt

426064358MFKGP

89 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: Schneider Medical GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426064358MFKGP
Device name: —
Device model: Mehrfachkompressen heiß/kalt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 5, 2025

Manufacturer & authorised representative

Manufacturer

Name: Schneider Medical GmbH
SRN: DE-MF-000005484
Country: Germany
Email: hello@schneider-medical.com
Phone: 49 (0) 7844 7051

Variants by status

UDI-DI variants

89 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1X5Y41YS0Q4H1NGC9TFS7FT

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

050A-0304260643580932
050B-0304260643580949
N/A04260643584664
N/A04260643584725
N/A04260643584657
N/A04260643584718
N/A04260643584640
N/A04260643584671
N/A04260643584688
N/A04260643584633
N/A04260643584695
N/A04260643584701
N/A04260643584794
N/A04260643582820

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