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Yellow Latex Finger Cot, Anti-static, Smooth, Rolled, Non sterile & Powder-free, Size M

by Komex Vina Co., Ltd.

Ref F200M

Active European Union

CE MDR

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/MDR Number8938539162F200Y9K Basic UDI-DI 08938539162123UDI-DIDate9 Aug 2025RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Yellow, plain, powder free, rolled latex finger cots, size M
Model / Reference
F200M
Primary DI / UDI-DI
08938539162123
Basic UDI-DI
8938539162F200Y9K
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
VN-MF-000007312
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Other devices from Komex Vina Co., Ltd.

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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