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Test Tube

by Yiwu Eason Medical Devices Co., Ltd. 9 variants

Ref 10mlΦ15*100ppModel Plastic Test Tube 3mlΦ12*60ps,5mlΦ12*75pp,5mlΦ13*75pp,5mlΦ12*75ps,5mlΦ13*75ps,7mlΦ12*100ps,7mlΦ13*100ps,10mlΦ15*100pp,10mlΦ16*100pp,10mlΦ16*102ps

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697734624TT01RE Basic UDI-DI 06977346241043UDI-DIDate24 Apr 2024RegisteredStatusActive

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  • Withdrawn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
Plastic Test Tube 3mlΦ12*60ps, 5mlΦ12*75pp, 5mlΦ13*75pp, 5mlΦ12*75ps, 5mlΦ13*75ps, 7mlΦ12*100ps, 7mlΦ13*100ps, 10mlΦ15*100pp, 10mlΦ16*100pp, 10mlΦ16*102ps
Primary DI / UDI-DI
06977346241043
Basic UDI-DI
697734624TT01RE
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000041286
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Yiwu Eason Medical Devices Co., Ltd.

See all devices from Yiwu Eason Medical Devices Co., Ltd. →

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