KLS Martin

by KLS Martin SE & Co. KG 1,000+ variants

Ref 09-004-63-07

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	Number40576053245D Basic UDI-DI 04057605374391UDI-DI	Date26 Sep 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Withdrawn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

Map note: Northern Ireland has no dot of its own.

Specification

EUDAMED

Device Name: Mallets
Model / Reference: 09-004-63-07

Primary DI / UDI-DI: 04057605374391
Basic UDI-DI: 40576053245D
EMDN Code: L0903 Orthopaedic surgery hammers, reusable

Device Class: Class I
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: DE-MF-000005551

From the manufacturer

Manufacturer's product page: Art.-Nr. 80-042-00-04 maXium® m-Version mit Buchsenmodul für KLS Martin-Zubehör

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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