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Scallop Abutment

by E-Pros Co., Ltd. EUDAMED

Active European Union

Ref EP-CL-CEModel SA-OSS6090NA

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08800155306499 Basic UDI-DIDate16 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Device Name
Scallop Abutment
Model / Reference
SA-OSS6090NA, EP-CL-CE
Primary DI / UDI-DI
08800155306499
Basic UDI-DI
B-08800155306499
EMDN Code
P01020101 Dental implants
Device Class
Class IIb
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