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Cellutec Pro

by SLEE medical GmbH Germany EUDAMED

Ref 11000700Model Tissue Processor Cellutec Pro

EMDN W02029099

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4260248680464WX Basic UDI-DIDate3 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Model / Reference
Tissue Processor Cellutec Pro, 11000700
Primary DI / UDI-DI
04260248680471
Basic UDI-DI
4260248680464WX
EMDN Code
W02029099 Various hematology / histology / cytology instruments - other
Device Class
Class A
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000041949

Other devices from SLEE medical GmbH

See all devices from SLEE medical GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Surgical Instrument
  • New Device
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No

Sources (1)

  • EUDAMED a65a666b-9f28-43b9-860b-c1b69d4c19f9 61 fields · synced 23 Oct 2026