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Bay Glove

by Trust Rubber Industry Co., Ltd. EUDAMED

Active European Union

Ref BGLPFM3302, BGLPFXS3300Model Single use device

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88594892000TRN6 Basic UDI-DIDate29 Dec 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Latex Powder Free Examination Gloves
Model / Reference
Single use device, BGLPFM3302, BGLPFXS3300
Primary DI / UDI-DI
08859489200027, 08859489200003
Basic UDI-DI
88594892000TRN6
Direct Marketing DI
08859489200027
08859489200003
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TH-MF-000007866
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Trust Rubber Industry Co., Ltd.

See all devices from Trust Rubber Industry 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