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Test Tube

by Jiangsu Kahotest Citotest Labware Manufacturing Co., Ltd 2 variants

Ref 16955257406000Model 12X75mm/13X75mm/12X100mm/13X100mm/15X100mm/16X100mm/16X102mm/16X125mm/16X150mm/40X200mm

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number69552574TT001U3 Basic UDI-DI 16955257406000UDI-DIDate15 May 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  • Withdrawn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
Test Tube
Model / Reference
12X75mm/13X75mm/12X100mm/13X100mm/15X100mm/16X100mm/16X102mm/16X125mm/16X150mm/40X200mm, 16955257406000
Primary DI / UDI-DI
16955257406000
Basic UDI-DI
69552574TT001U3
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
CN-MF-000034323
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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Properties

  • Professional Testing

Other properties (10)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No