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White latex finger cots, Powdered, Rolled, Smooth, Non sterile, size M

by Komex Vina Co., Ltd. 2 variants

Ref F100M

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8938539162F100AL Basic UDI-DI 08938539162024UDI-DIDate23 May 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  • Withdrawn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
White latex finger cots, Powdered, Rolled, Smooth and Non sterile
Model / Reference
F100M
Primary DI / UDI-DI
08938539162024
Basic UDI-DI
8938539162F100AL
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