Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

KÄLTE SOFRT Kompresse neu 15x25cm — Class I MDR

MD Atlas
C+V Pharma Depot GmbH

EUDAMED last updated this device on May 25, 2026

KÄLTE SOFRT Kompresse neu 15x25cm

PP05199KSK68

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C+V Pharma Depot GmbH
UDI-DI code: 112019058695
Reference / catalog number: 11201905869500

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

Organization name: C+V Pharma Depot GmbH
SRN: DE-MF-000022382
Manufacturer status: Active

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW011
Nur zur äußerlichen Anwendung, direkten Hautkontakt vermeiden, vor Kindern unzugänglich aufbewahren
CW010
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Netherlands		Still on market

Device identification

Trade name: KÄLTE SOFRT Kompresse neu 15x25cm
UDI-DI code: 112019058695
Basic UDI-DI: PP05199KSK68
Reference / catalog number: 11201905869500
Issuing entity: IFA

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Het koud kompres voor direct gebruik is een medisch hulpmiddel voor eenmalig uitwendig gebruik op een intacte huid, voor verlichting en behandeling van pijn en zwellingen in ziekenhuizen, medische praktijken, thuis of in de vrije tijd.
Additional information URL: https://cuv.copiki.de/w/C%2BV_Pharma
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M9001CRYOTHERAPY AND THERMOTHERAPY DEVICES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas

Related devices

A00001511PP05199E.GEL58On the market A00001209PP05199E.GEL58On the market A00001149PP05199E.GEL58On the market E-Gel 250 g Henry Schein HSPP05199E.GEL58On the market A00001204PP05199E.GEL58On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.