Multiflex Ext. Foot Prosthesis 26 Right

by Blatchford Products Limited

Ref 519128

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	Number5050649MULTIFLEXSTD9X Basic UDI-DI 05050649012389UDI-DI	Date10 Nov 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Withdrawn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: Multiflex
Model / Reference: 519128

Primary DI / UDI-DI: 05050649012389
Basic UDI-DI: 5050649MULTIFLEXSTD9X
EMDN Code: Y062409 Transtibial prostheses (for amputation under knee)

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: UK-MF-000048777
Authorised representative: Blatchford Europe GmbH DE-AR-000006292

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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