Nociceptol® Schmerzlinderndes Gel

by Laboratoire Polidis 2 variants

Ref 5814090

Active European Union

CE MDR

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number3664538ADGL01NLQB Basic UDI-DI 03664538000511UDI-DI	Date22 Aug 2024Registered	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Withdrawn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/MDR Active

Specification

EUDAMED

Device Name: Nociceptol Gel Anti-Douleur
Model / Reference: 5814090

Primary DI / UDI-DI: 03664538000511
Basic UDI-DI: 3664538ADGL01NLQB
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Austria

Manufacturer details

EUDAMED SRN: FR-MF-000004550

Other devices from Laboratoire Polidis

Pain relief Cold Gel (headaches)

Class I
Pain relief Solution

Class I
Head lice and nits shampoo

Class IIa
Nits remover

Class I
Pain relief Cold Gel

Class I
Myocalm

Class I

See all devices from Laboratoire Polidis →

Properties

Other properties (13)

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