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Neobone

by Bioceramed - Cerâmicos Para Aplicações Médicas, S.A. 24 variants

Ref GN510, G020420, B1030101, G0204025, B1030053, B1010055, B1010201, B1010203, G040620, B1515205, G020410, B1030051, GN420, B1515303, G020405, B1030105, B1515301, B1010053, B2020101, C2015081Model biphasic7525

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05600870020846 Basic UDI-DI Date22 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Neobone
Model / Reference
biphasic7525, GN510, G020420, B1030101, G0204025, B1030053, B1010055, B1010201, B1010203, G040620, B1515205, G020410, B1030051, GN420, B1515303, G020405, B1030105, B1515301, B1010053, B2020101, C2015081
Primary DI / UDI-DI
05600870020846, 05600269575674, 05600269575391, 05600269575742, 05600269575377, 05600269575353, 05600269575278, 05600269575285, 05600269575728, 05600269575230, 05600269575650, 05600269575360, 05600870020822, 05600269575254, 05600269575643, 05600269575414, 05600269575247, 05600269575346, 05600269575186, 05600269575476
Basic UDI-DI
B-05600870020846, B-05600269575674, B-05600269575391, B-05600269575742, B-05600269575377, B-05600269575353, B-05600269575278, B-05600269575285, B-05600269575728, B-05600269575230, B-05600269575650, B-05600269575360, B-05600870020822, B-05600269575254, B-05600269575643, B-05600269575414, B-05600269575247, B-05600269575346, B-05600269575186, B-05600269575476
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002812

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Properties

  • Sterile
  • Implantable

Other properties (9)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No