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MEDOJECT 1, 2x50mm with filter (18G x 2”)

by CHIRANA T.Injecta, a.s.

Ref CH18200FModel Blunt fill needle

Expiring European Union

CE MDR

Valid until

30 Sep 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier 3EC International a.s.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number858601504BFNEEDLE24SV Basic UDI-DI 08586015045325UDI-DIDate5 Jun 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 2022-MDR/QS-024/B Expiring Supplemented Expires in 333 days

    Quality management system EU MDR

    Certifier
    3EC International a.s. 2265
    Issued
    28 May 2026
    Expires
    30 Sep 2027
    Reason
    Change approved

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Expiring

Specification

EUDAMED

Device Name
Sterile blunt fill needle for single use
Model / Reference
Blunt fill needle, CH18200F
Primary DI / UDI-DI
08586015045325
Basic UDI-DI
858601504BFNEEDLE24SV
Direct Marketing DI
08586015045325
EMDN Code
A019001 Blunt needles
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
SK-MF-000003702

Other devices from CHIRANA T.Injecta, a.s.

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Properties

  • Sterile
  • Administering Medicine

Other properties (11)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No