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Natriumcitrat Lösung 3, 13% 50 x 2 ml

by Eifelfango Chem. Pharm. Werk GmbH & Co. KG Germany EUDAMED

Ref IFA EMDN W01030107

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberPP07140NATRI07 Basic UDI-DIDate29 Jan 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  • Withdrawn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
Natriumcitrat Lösung 3,13% 10x1ml
Model / Reference
IFA
Primary DI / UDI-DI
110070274210
Basic UDI-DI
PP07140NATRI07
Direct Marketing DI
110070274210
EMDN Code
W01030107 Erythrocyte sedimentation rate (esr) test
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000009424

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Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Reagent
  • Professional Testing
Other properties (8)
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 18f12e5a-ca95-40ab-80d7-4498e2ef3662 61 fields · synced 24 Oct 2026