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by My Ti̇caret Ve Medi̇kal Anoni̇m Şi̇rketi̇ 6 variants

Ref SELPF01-S, SELPP02-M, SELPP03-L

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868302002LPFLR Basic UDI-DI Date24 May 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  • Withdrawn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 Powderfree Examination Gloves
Latex Powdered Examination Gloves
Model / Reference
SELPF01-S, SELPP02-M, SELPP03-L
Primary DI / UDI-DI
08683020023109, 08683020023055, 08683020023062
Basic UDI-DI
868302002LPFLR, 868302002LPVJ
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000018372

Other devices from My Ti̇caret Ve Medi̇kal Anoni̇m Şi̇rketi̇

See all devices from My Ti̇caret Ve Medi̇kal Anoni̇m Şi̇rketi̇ →

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