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Arthrex®

by Arthrex Inc. United States EUDAMED

Ref ABS-10066Model ANGEL PRP SYSTEM CENTRIFUGE EU (NEW)

EMDN B0501

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-00888867084025 Basic UDI-DIDate2 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Model / Reference
ANGEL PRP SYSTEM CENTRIFUGE EU (NEW), ABS-10066
Primary DI / UDI-DI
00888867084025
Basic UDI-DI
B-00888867084025
EMDN Code
B0501 Platelet gel automatic preparation devices (excluding bags)
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
US-MF-000019271
Authorised representative
Arthrex GmbH DE-AR-000016163

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 00888867084025|B-00888867084025 61 fields · synced 25 Oct 2026