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Diagnostic Consumable Kit Ziehl Neelsen (ZN) V4

by Svizera Europe BV EUDAMED

Withdrawn Not intended for the EU market

Ref Diagnostic Consumable Kit Ziehl Neelsen (ZN) V4

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number872076967ZNV4ST Basic UDI-DIDate27 May 2025RegisteredStatusWithdrawn Not intended for the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Withdrawn

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Diagnostic Consumable Kit Ziehl Neelsen (ZN) V4
Model / Reference
Diagnostic Consumable Kit Ziehl Neelsen (ZN) V4
Primary DI / UDI-DI
08707696700024
Basic UDI-DI
872076967ZNV4ST
EMDN Code
W0102010101 Immunoglobulin a
Device Class
Class A

Manufacturer details

EUDAMED SRN
NL-MF-000047495

Properties

  • Reagent
  • Professional Testing
  • Companion Diagnostics
  • Surgical Instrument
  • New Device

Other properties (6)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No