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ROTANTA 460 RF, 200-240V 50Hz

by Andreas Hettich GmbH EUDAMED

Active European Union

Ref 5675-50Model 5650, 5660, 5670, 5675

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number040506740100039N Basic UDI-DIDate16 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Rotanta 460
Model / Reference
5650, 5660, 5670, 5675, 5675-50
Primary DI / UDI-DI
04050674067539
Basic UDI-DI
040506740100039N
Direct Marketing DI
04050674067539
EMDN Code
W02069005 Refrigerated centrifuges
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000010680

From the manufacturer

Manufacturer's product page: ROTANTA 460 | 460 R

Other devices from Andreas Hettich GmbH

See all devices from Andreas Hettich GmbH →

Properties

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