E Pro Skinotopiq Med Krem Do Ciała

by LABORATOIRE L'IDEAL Parisien Sp. z o.o. 2 variants

Ref E PRO SKINOTOPIQ MED KREM DO CIAŁA Product packed in a 500g jar, Polish language version

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDD	NumberB-05904335216370 Basic UDI-DI 05904335216370UDI-DI	Date6 May 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name: Atopic skin cream / Krem do skóry atopowej
Model / Reference: E PRO SKINOTOPIQ MED KREM DO CIAŁA Product packed in a 500g jar, Polish language version

Primary DI / UDI-DI: 05904335216370
Basic UDI-DI: B-05904335216370
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Poland

Manufacturer details

EUDAMED SRN: PL-MF-000005402

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Properties

Other properties (11)

Sterile: No
Implantable: No
Reusable: No
Contains Latex: No
Reprocessed: No
Human-derived: No
Human Tissues: No
Animal Tissues: No
Administering Medicine: No
Measuring Function: No
Incorporates Medicinal Product: No