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Hunan Biojoint Instrument Co., Ltd

by Hunan Biojoint Instrument Co., Ltd 211 variants

Ref P10AModel 0.1ml ,0.2ml, 1.5ml, 2ml,5ml,10ml,15ml,50ml, DS20,DR20,P60A,P30A,P20A,P15A,P10A, CS

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 Number697836720CentrifugeTubePW Basic UDI-DI 06978367202235UDI-DIDate10 Mar 2025RegisteredStatusActive

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  • Withdrawn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, 1.5ml, 2ml, 5ml, 10ml, 15ml, 50ml, DS20, DR20, P60A, P30A, P20A, P15A, P10A, CS
Primary DI / UDI-DI
06978367202235
Basic UDI-DI
697836720CentrifugeTubePW
EMDN Code
W0599 IVD general use consumable devices - other
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000046607
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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Properties

  • New Device

Other properties (10)

  • 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