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Desiccant tube

by Cangzhou Shengfeng Plastic Product Co., Ltd

Ref 3mlModel 3ml; 5ml; 10ml;15ml;20ml;30ml;50ml;100ml;200ml;300ml;500ml;1000ml;2000ml

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 Number698031904DT001A6 Basic UDI-DI 06980319041809UDI-DIDate27 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Desiccant tube
Model / Reference
3ml, 5ml, 10ml, 15ml, 20ml, 30ml, 50ml, 100ml, 200ml, 300ml, 500ml, 1000ml, 2000ml
Primary DI / UDI-DI
06980319041809
Basic UDI-DI
698031904DT001A6
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000020600
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Cangzhou Shengfeng Plastic Product 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