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Haspet Latex Examination Gloves Powdered Xlarge

by N Ve H Medikal Ithalat Ihracat Pazarlama Ve Ticaret Anonim Sirketi 5 variants

Ref PWMDR268XL

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868036179PWMDR268KQ Basic UDI-DI 08680361793111UDI-DIDate25 Sep 2026RegisteredStatusActive

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  • Withdrawn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
Haspet Latex Examination Gloves Powdered
Model / Reference
PWMDR268XL
Primary DI / UDI-DI
08680361793111
Basic UDI-DI
868036179PWMDR268KQ
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000039027

Other devices from N Ve H Medikal Ithalat Ihracat Pazarlama Ve Ticaret Anonim Sirketi

See all devices from N Ve H Medikal Ithalat Ihracat Pazarlama Ve Ticaret Anonim Sirketi →

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