Skip to content

Glyde Pro Ultra

by Richter Rubber Technology Sdn Bhd 3 variants

Ref QA-224

Active European Union

CE MDR

Valid until

6 Feb 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier SGS Belgium NV

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMY26/00000108 Date6 Feb 2026IssuedStatusActive expires 6 Feb 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MY26/00000108 Active

    Quality management system EU MDR

    Certifier
    SGS Belgium NV 1639
    Issued
    6 Feb 2026
    Expires
    6 Feb 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Non-Medicated Natural Latex Condoms
Model / Reference
QA-224
Primary DI / UDI-DI
09556807500898
Basic UDI-DI
9556807CD001UF
Direct Marketing DI
09556807500898
EMDN Code
U110101 Condoms
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
MY-MF-000023324
Authorised representative
rrt Vertrieb und Service GmbH DE-AR-000021443

Other devices from Richter Rubber Technology Sdn. Bhd.

See all devices from Richter Rubber Technology Sdn. Bhd. →

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