Skip to content

Misch-Stäbchen für SC-Kunststoff-Blutgaskapillaren, 0, 7 x 9 mm

by SC - Sanguis Counting Kontrollblutherstellungs- und Vertriebs GmbH

Ref 110007

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 Number426015999601BB Basic UDI-DI 04260159990317UDI-DIDate27 Aug 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  • Withdrawn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
Zubehör
Model / Reference
110007
Primary DI / UDI-DI
04260159990317
Basic UDI-DI
426015999601BB
Direct Marketing DI
04260159990317
EMDN Code
W050180 Samples collection devices - other accessories
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000023385

From the manufacturer

Manufacturer's product page: Sechskant-Verschlusskappen für SC-Kunststoff-Blutgaskapillaren

Other devices from SC - Sanguis Counting Kontrollblutherstellungs- und Vertriebs GmbH

See all devices from SC - Sanguis Counting Kontrollblutherstellungs- und Vertriebs GmbH →

Properties

Other properties (11)

  • 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
  • New Device: No