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Slit Hammer

by Hoogland Spine Products GmbH

Ref 1001-AI 006Model Hammer

Slit Hammer (1001-AI 006) is a Class I device made by Hoogland Spine Products, GmbH, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 426020031MaxmoreHammerCL), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426020031MaxmoreHammerCL Basic UDI-DI 04260200314123UDI-DIDate4 Nov 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Hammer, 1001-AI 006
Primary DI / UDI-DI
04260200314123
Basic UDI-DI
426020031MaxmoreHammerCL
EMDN code
L0903 Orthopaedic surgery hammers, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000011261

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY HAMMERS, REUSABLE.

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Properties

  • Sterilise before use
Other properties (13, all answered No)