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Bonescreen GmbH

Germany DE-MF-000036576 Last updated 8 Jun 2026

Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

  • SpineQ Ref SpineQ v2.0.1

    Class IIa EUDAMED Active
  • SpineQ Ref SpineQ v1.3.0

    Class IIa EUDAMED Active
  • SpineQ Ref SpineQ

    Class IIa EUDAMED Active
  • SpineQ Ref SpineQ v1.1.0

    Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

Notified body 0633 1 certificate

  • Z-24-007-S-E Issued

    Quality management system EU MDR

    Issued
    6 Jun 2025
    Expires
    5 Jun 2030

Notified bodies

  • Notified body 0633

Information

Country
Germany
Address
34, Orleansstraße, München, Germany
Website
bonescreen.de
PRRC contact
Jan Kirschke
EUDAMED SRN
DE-MF-000036576