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HASPET Latex Examination Gloves Powder Free Medium

by N Ve H Medikal Ithalat Ihracat Pazarlama Ve Ticaret Anonim Sirketi 9 variants

Ref PFMDRW14M

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 Number868036179PFMDRW14FL Basic UDI-DI 08680361796204UDI-DIDate22 Aug 2024RegisteredStatusActive

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  • Withdrawn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 Powder Free
Model / Reference
PFMDRW14M
Primary DI / UDI-DI
08680361796204
Basic UDI-DI
868036179PFMDRW14FL
Direct Marketing DI
08680361796204
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