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Latex examination powder free gloves

by Lalan Rubbers (Pvt) Ltd. 8 variants

Ref LE 002- Size 6

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

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 Number479602973479602973333874 Basic UDI-DI 47960297327062UDI-DIDate20 Oct 2025RegisteredStatusWithdrawn No longer placed on the EU market

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Specification

EUDAMED

Device Name
Latex examination powder free gloves
Model / Reference
LE 002- Size 6
Primary DI / UDI-DI
47960297327062
Basic UDI-DI
479602973479602973333874
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I

Manufacturer details

EUDAMED SRN
LK-MF-000033196
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Lalan Rubbers (Pvt) Ltd.

See all devices from Lalan Rubbers (Pvt) Ltd. →

Properties

  • Sterile
  • Contains Latex
  • Administering Medicine

Other properties (10)

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