HandyFix

by HandyLegs B.V. 3 variants

Ref HandyFix V2

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	Number2866258HFV2-XJ Basic UDI-DI 08720892694003UDI-DI	Date10 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Withdrawn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

Model / Reference: HandyFix V2

Primary DI / UDI-DI: 08720892694003
Basic UDI-DI: 2866258HFV2-XJ
Direct Marketing DI: 08720892694003
EMDN Code: M030499 Elastic bandages, support and compression - other

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: NL-MF-000023821

Other devices from HandyLegs B.V.

HandyLegs 1

Class I
HandyFix

Class I
HandyLegs 2

Class I
HandyHold Extra Large

Class I
HandyHold Medium

Class I
HandyHold Extra extra large

Class I

See all devices from HandyLegs B.V. →

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