Nord Liner Tf Conical - Type 3.2 Nf-53

by Nord Ability AB 8 variants

Ref 322238Model NORD LINER TF CUSHION

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number73501284936PC Basic UDI-DI 07350128496197UDI-DI	Date13 Apr 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Withdrawn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: NORD LINER TF CUSHION – Available in TYPE 3.1 NF-53 (Cylindrical) and TYPE 3.2 NF-53 (Conical)
Model / Reference: NORD LINER TF CUSHION, 322238

Primary DI / UDI-DI: 07350128496197
Basic UDI-DI: 73501284936PC
EMDN Code: Y062415 Transfemoral prostheses (for amputation above knee)

Device Class: Class I
EU market of registration: Sweden

Manufacturer details

EUDAMED SRN: SE-MF-000002255

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Nord Liner Tf Conical - Type 3.2 Nf-53

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Nord Sleeve - Type 1.1 Nf-29

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See all devices from Nord Ability AB →

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