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Centrifuge Tube

by Nantong Yuanyi experimental Equipment CO., LTD

Ref 0.1mlModel 0.1ml 0.2ml 0.5ml 1.5ml 2ml 5ml 7ml 10ml 15ml 25ml 30ml 50ml 100ml 120ml 150ml

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697682018YYCT022P Basic UDI-DI 06976820181004UDI-DIDate2 Nov 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Centrifuge Tube
Model / Reference
0.1ml 0.2ml 0.5ml 1.5ml 2ml 5ml 7ml 10ml 15ml 25ml 30ml 50ml 100ml 120ml 150ml, 0.1ml
Primary DI / UDI-DI
06976820181004
Basic UDI-DI
697682018YYCT022P
Direct Marketing DI
06976820181004
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000038319
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Nantong Yuanyi experimental Equipment CO., LTD

Properties

Other properties (11)

  • 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
  • Surgical Instrument: No
  • New Device: No