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Tulipán Frutilla Condom Rubber Latex Natural

by Thai Nippon Rubber Industry Public Company Limited

Ref KOPARG-011

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88529610TNRC01YQ Basic UDI-DI 18852961034698UDI-DIDate27 Nov 2023RegisteredStatusActive

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  • Withdrawn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
Natural Rubber Latex Non-Medicated Male Condom
Model / Reference
KOPARG-011
Primary DI / UDI-DI
18852961034698
Basic UDI-DI
88529610TNRC01YQ
Direct Marketing DI
18852961034698
EMDN Code
U110101 Condoms
Device Class
Class IIb
EU market of registration
Spain

Manufacturer details

EUDAMED SRN
TH-MF-000012641
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Thai Nippon Rubber Industry Public Company Limited

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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