Knee Bandage

by Spronken Orthopedie 2 variants

Ref NF-KNIEBANDAGE-ZWART, NF-KNIEBANDAGE-COLD2

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	Number1169154KNE04PW Basic UDI-DI	Date16 Feb 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Withdrawn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: Knee Bandage
Model / Reference: NF-KNIEBANDAGE-ZWART, NF-KNIEBANDAGE-COLD2

Primary DI / UDI-DI: 08720589780132, 08720589780125
Basic UDI-DI: 1169154KNE04PW
EMDN Code: Y061209 Knee orthoses

Device Class: Class I
EU market of registration: Belgium

Manufacturer details

EUDAMED SRN: BE-MF-000003430

Other devices from Spronken Orthopedie

Hip Bandage

Class I
Jaw Bandage

Class I
S-UOMO Brace

Class I
Knee Bandage

Class I
Shoulder Bandage

Class I
Hip Bandage

Class I

See all devices from Spronken Orthopedie →

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