Rodillera Abierta Reforzada Neopreno

by Dyno Rechi 3 variants

Ref 0516001S07

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number843582590516002M07RP Basic UDI-DI 08435825900778UDI-DI	Date29 Sep 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Withdrawn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

Model / Reference: 0516001S07

Primary DI / UDI-DI: 08435825900778
Basic UDI-DI: 843582590516002M07RP
EMDN Code: Y061209 Knee orthoses

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: ES-MF-000035525

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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