HandyHold Large

by HandyLegs B.V.

Ref HandHold LargeModel HandyHold

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number2866258HHV06B Basic UDI-DI 08720892694041UDI-DI	Date23 Mar 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Withdrawn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: HandyHold
Model / Reference: HandyHold, HandHold Large

Primary DI / UDI-DI: 08720892694041
Basic UDI-DI: 2866258HHV06B
Direct Marketing DI: 08720892694041
EMDN Code: M030405 Compression stockings

Device Class: Class I
EU market of registration: Netherlands

Manufacturer details

EUDAMED SRN: NL-MF-000023821

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HandyHold Extra extra large

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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