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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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Kälte-Sofort-Kompresse — 4 UDI-DI variants, MDR

MD Atlas
C+V Pharma Depot GmbH

Data from EUDAMED, last updated May 23, 2026

Kälte-Sofort-Kompresse

PP05199KSK68

4 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: C+V Pharma Depot GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP05199KSK68
Device name: Kälte-Sofort-Kompresse
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 21, 2024

Manufacturer & authorised representative

Manufacturer

Name: C+V Pharma Depot GmbH
SRN: DE-MF-000022382
Country: Germany
Email: qm@cundv.de

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JD7Q5SZV8VK73690VP7KB7BF

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

11193799763800111937997638
11193800050500111938000505
KÄLTE SOFORT Kompresse neu 15x17cm112019055776
KÄLTE SOFRT Kompresse neu 15x25cm112019058695