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Serix Navy

by Tg Medical Sdn. Bhd. 5 variants

Ref MED-100419133

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, self-declared

Class I: no certifier involved

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 Number955583993480QU Basic UDI-DI 09551004191337UDI-DIDate25 Jul 2022RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Latex Examination Powder Free Gloves
Model / Reference
MED-100419133
Primary DI / UDI-DI
09551004191337
Basic UDI-DI
955583993480QU
Direct Marketing DI
09551004191337
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
MY-MF-000009606
Authorised representative
Ulma International GmbH DE-AR-000010015

Other devices from Tg Medical Sdn. Bhd.

See all devices from Tg Medical 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