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Latex Examination Pre Powdered Gloves

by Lalan Rubbers (Pvt) Ltd.

Ref LE 001- Size 8.5

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 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 Number47960297347960297334066U Basic UDI-DI 47960297325464UDI-DIDate20 Oct 2025RegisteredStatusActive

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  • Withdrawn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 Active

Specification

EUDAMED

Device Name
Latex Examination Pre Powdered Gloves
Model / Reference
LE 001- Size 8.5
Primary DI / UDI-DI
47960297325464
Basic UDI-DI
47960297347960297334066U
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