Skip to content

Scallop Abutment

by E-Pros Co., Ltd. 136 variants

Ref EP-CL-CEModel SA-OSS7080HB

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800155306567 Basic UDI-DI 08800155306567UDI-DIDate19 Oct 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  • Withdrawn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
Scallop Abutment
Model / Reference
SA-OSS7080HB, EP-CL-CE
Primary DI / UDI-DI
08800155306567
Basic UDI-DI
B-08800155306567
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
KR-MF-000030823
Authorised representative
SOAR & PARTNERS Sp. z o.o. PL-AR-000040956

Other devices from E-Pros Co., Ltd.

See all devices from E-Pros Co., Ltd. →

Properties

  • Implantable

Other properties (10)

  • Sterile: No
  • 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