Skip to content

DexPure 803-88

by PIP Global Safety France

Ref 4580388, 45 803-88 10-XL, 45 803-88 8-M, 45 803-88 9-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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number360383458038188GF Basic UDI-DI Date21 Sep 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  • Withdrawn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
DexPure 803-81
Model / Reference
4580388, 45 803-88 10-XL, 45 803-88 8-M, 45 803-88 9-L
Primary DI / UDI-DI
13603835713264, 13603835714438, 13603835714124, 13603835714131
Basic UDI-DI
360383458038188GF
Direct Marketing DI
13603835713264
13603835714438
13603835714124
13603835714131
EMDN Code
T01020204 Nitrile examination / treatment gloves
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000023170

Other devices from PIP Global Safety France

See all devices from PIP Global Safety France →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: 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