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Specimen collection swab

by Medico Technology Co., Ltd 33 variants

Ref MFS-96000BQ-RModel MFS-96000BQ

Active European Union

CE MDR

Valid until

28 Nov 2027

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier Intertek Medical Notified Body AB

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/MDR Number28620139275-01 Date6 Mar 2026IssuedStatusActive expires 28 Nov 2027

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Specimen collection swab
Model / Reference
MFS-96000BQ, MFS-96000BQ-R
Primary DI / UDI-DI
06974931650587
Basic UDI-DI
697493165SCSWU
EMDN Code
A1101 Sample collection neutral swabs
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000013067
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Medico Technology Co., Ltd

See all devices from Medico Technology Co., Ltd →

Properties

  • Sterile

Other properties (12)

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