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capillary tube 10/20ul(Blue/Black, 2 line)

by HLB Life Science Co., LTD

Ref HLB-CBT1020UL-25AModel Capillary tube 10/20ul (Blue/Black, 2 line)

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number880989962CBT04R3 Basic UDI-DI 08809899620236UDI-DIDate6 May 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  • Withdrawn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
Capillary tube 10/20ul (Blue/Black, 2 line)
Model / Reference
Capillary tube 10/20ul (Blue/Black, 2 line), HLB-CBT1020UL-25A
Primary DI / UDI-DI
08809899620236
Basic UDI-DI
880989962CBT04R3
EMDN Code
W0501010203 Blood collection, capillary tubes
Device Class
Class A
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
KR-MF-000031817
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Hlb Lifescience Co., Ltd.

See all devices from Hlb Lifescience 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