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Mini-tip QP type 10ul (with plunger)

by HLB Life Science Co., LTD

Ref HLB-MNTQP10UL-1AModel Mini-tip QP type 10ul (with plunger)

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 Number880989962CBT11QY Basic UDI-DI 08809899620755UDI-DIDate7 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  • Withdrawn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

Model / Reference
Mini-tip QP type 10ul (with plunger), HLB-MNTQP10UL-1A
Primary DI / UDI-DI
08809899620755
Basic UDI-DI
880989962CBT11QY
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 Life Science Co., LTD

See all devices from HLB Life Science 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