Skip to content

Hygro-L ALIF-MBW H18

by privelop-spine ag

Ref 2021-1006Model Hygro-Cage

Active European Union

CE MDR

Valid until

3 Apr 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number764014104A11AJ Basic UDI-DI 07640141044056UDI-DIDate19 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20406GB450240404 Active

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    4 Apr 2024
    Expires
    3 Apr 2029

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Hygro-L ALIF-MBW H24
Model / Reference
Hygro-Cage, 2021-1006
Primary DI / UDI-DI
07640141044056
Basic UDI-DI
764014104A11AJ
EMDN Code
P09070101 Spinal cages
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000027580
Authorised representative
privelop AG DE-AR-000005634

Other devices from privelop-spine ag

See all devices from privelop-spine ag →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • 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