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SINOSSBONE GRANULES 0.5 g - 200-600 micron

by B. & B. Dental S.r.l.

Ref SBG-0.5

Active European Union

CE MDR

Valid until

27 Nov 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier ISTITUTO SUPERIORE DI SANITA'

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberCSQ0015230226 Date8 Jun 2026IssuedStatusActive expires 27 Nov 2028

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • CSQ0015230226 Active Supplemented

    Quality management system EU MDR

    Issued
    8 Jun 2026
    Expires
    27 Nov 2028
    Reason
    Add device or group
  • CVD0021230226 Active Supplemented

    Technical documentation EU MDR

    Issued
    8 Jun 2026
    Expires
    27 Nov 2028
    Reason
    Add device or group

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Novobone Granules
Model / Reference
SBG-0.5
Primary DI / UDI-DI
80594937806874
Basic UDI-DI
805228249BOVINENOVOBONE5G
EMDN Code
P900401 Bone and tendon replacement devices
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000028342

Other devices from B. & B. Dental S.r.l.

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Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No