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Needle Placer

by Hoogland Spine Products GmbH

Ref 99-999-97Model Needle Placer

Needle Placer (99-999-97) is a Class I device made by Hoogland Spine Products, GmbH, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 426020031MaxmoreNPH4C), 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 Number426020031MaxmoreNPH4C Basic UDI-DI 04260200314444UDI-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  • Withdrawn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
Needle Placer, 99-999-97
Primary DI / UDI-DI
04260200314444
Basic UDI-DI
426020031MaxmoreNPH4C
EMDN code
A018002 Needle guides
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000011261

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Properties

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