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F. Bosch Vinyl Protective/Examination Gloves Blue Powdered M

by F. Bosch International Limited

Ref FBGLVE-2033

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 Number489714698FBGLVEVINYLWB Basic UDI-DI 04897146980534UDI-DIDate21 Dec 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  • Withdrawn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
Vinyl Examination Glove
Model / Reference
FBGLVE-2033
Primary DI / UDI-DI
04897146980534
Basic UDI-DI
489714698FBGLVEVINYLWB
Direct Marketing DI
04897146980534
EMDN Code
T01020201 Vinyl examination / treatment gloves
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
HK-MF-000029001
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from F. Bosch International Limited

See all devices from F. Bosch International Limited →

Properties

Other properties (13)

  • Sterile: No
  • 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