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Zestaw Do Ob P-3

by Aquisel S.L.U. Spain EUDAMED

Ref 7010321000Model AQUISEL Erythrocyte Sedimentation Rate Devices EMDN W02029001

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8429889-TF-2000-M2 Basic UDI-DIDate15 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Erythrocyte Sedimentation Rate Devices (ESR)
Model / Reference
AQUISEL Erythrocyte Sedimentation Rate Devices, 7010321000
Primary DI / UDI-DI
08429889002141
Basic UDI-DI
8429889-TF-2000-M2
EMDN Code
W02029001 Erythrocyte sedimentation rate devices
Device Class
Class A
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000020750

Other devices from Aquisel S.L.U.

See all devices from Aquisel S.L.U. →

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
Other properties (10)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 08429889002141|8429889-TF-2000-M2 61 fields · synced 24 Oct 2026