Plantilla Diabeflex Talla 39/40

Ref 7500TPR 39/40

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	Number843551567500TPRXL Basic UDI-DI 08435515600063UDI-DI	Date31 Mar 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Withdrawn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: Plantilla Diabeflex
Model / Reference: 7500TPR 39/40

Primary DI / UDI-DI: 08435515600063
Basic UDI-DI: 843551567500TPRXL
EMDN Code: Y061203 Orthoses, foot (including insoles and inserts)

Device Class: Class I
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: ES-MF-000042891

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Properties

Contains Latex

Other properties (12)

Sterile: No
Implantable: No
Reusable: 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