Bromellin Gel

by Winform Medical Engineering S.R.L.

Ref CBRL5002Model Dispositivo medico in gel

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number805210967DMGEL73 Basic UDI-DI 08052109670051UDI-DI	Date4 Jun 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Withdrawn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/MDR Active

Specification

EUDAMED

Device Name: Arnilin Gel
Model / Reference: Dispositivo medico in gel, CBRL5002

Primary DI / UDI-DI: 08052109670051
Basic UDI-DI: 805210967DMGEL73
EMDN Code: V9099 Various devices not included in other classes - other

Device Class: Class I
EU market of registration: Italy

Manufacturer details

EUDAMED SRN: IT-MF-000031384

Other devices from Winform Medical Engineering S.R.L.

Fillerjalux Gel

Class I
Gel HC500

Class I
High Performance Tecar Cream

Class I
Artrosikjalux Gel

Class I
Demusco Gel

Class I
Life Gel

Class I

See all devices from Winform Medical Engineering S.R.L. →

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