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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-Kompresse — 6 UDI-DI variants, MDR (Sportomed GmbH)

MD Atlas
Sportomed GmbH

Data from EUDAMED, last updated May 23, 2026

Kalt-/Warm-Kompresse

PP27855KWKOMPRESSE27

6 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: Sportomed GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP27855KWKOMPRESSE27
Device name: Kalt-/Warm-Kompresse
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Sportomed GmbH
SRN: DE-MF-000006642
Country: Germany
Email: info@roewo.de
Phone: 08 00 - 2 03 30 50

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J03QYA0S4TKNGS6JSV1GBS4M

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

62403111963086745
62239 / 62403111667594121
69410 / 69461111793320427
205031110424245086
302547111692602441
302546111692603007