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Endobon® Bovine Xenograft Moldable

by MedPark Co., Ltd. 7 variants

Ref ENXM05Model S1-XB-P025 (ENXM05)

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-S1-XB-P025(ENXM05)78 Basic UDI-DI D-S1-XB-P025(ENXM05)78UDI-DIDate21 Jul 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  • Withdrawn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

Model / Reference
S1-XB-P025 (ENXM05), ENXM05
Primary DI / UDI-DI
D-S1-XB-P025(ENXM05)78
Basic UDI-DI
B-S1-XB-P025(ENXM05)78
EMDN Code
Q010302 Dental graft devices
Device Class
Class III
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000016913
Authorised representative
Meridius Medical Europe Limited IE-AR-000004258

Other devices from Medpark Co., Ltd.

See all devices from Medpark Co., Ltd. →

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (8)

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