Fisioprim Gel Frío Para El Dolor

by Laboratoire Polidis 2 variants

Ref 8434048536580

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number3664538ADGL04PRRC Basic UDI-DI 08434048536580UDI-DI	Date30 Jul 2025Registered	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Withdrawn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: Fisioprim Gel Frio
Model / Reference: 8434048536580

Primary DI / UDI-DI: 08434048536580
Basic UDI-DI: 3664538ADGL04PRRC
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Portugal

Manufacturer details

EUDAMED SRN: FR-MF-000004550

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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