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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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Kalt-/Warm-Kompressen — 19 UDI-DI variants, MDR

MD Atlas
PS Product Services GmbH

Data from EUDAMED, last updated May 23, 2026

Kalt-/Warm-Kompressen

4050235PS0003BE

19 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: PS Product Services GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4050235PS0003BE
Device name: Kalt-/Warm-Kompressen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 7, 2021

Manufacturer & authorised representative

Manufacturer

Name: PS Product Services GmbH
SRN: DE-MF-000005290
Country: Germany
Email: ulla.kaltenbach@product-services.de

Variants by status

UDI-DI variants

19 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FPANGHG727Y3SQ1XBEJZYJMX

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

TS007904050235003907
TS007904050235003914
TS005604050235000777
TS005504050235000739
TS005404050235000692
TS004104050235000425
TS003904050235000364
TS003904050235000357
TS006104050235001620
TS006104050235001637
TS006204050235001569
Vitalis04050235000395
TS006904050235002412
Vitalis04050235000388
TS006204050235001606
TS004104050235000418
TS006004050235001590
TS006904050235002405
TS006204050235001576