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P.O.L. RX Crema (100 ml)

by Difa Cooper S.p.A.

Ref 420557 100 ml

Active European Union

CE MDR

Valid until

12 Dec 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

2 certificates

Certifier Eurofins Product Testing Italy S.r.l.

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 Number3271536123PN9 Basic UDI-DI 08032715360010UDI-DIDate7 Sep 2026RegisteredStatusActive

Certificates

2 certificates · EUDAMED

EUDAMED certificates (2)
  • EPT 0477.MDR.24/5668 Active

    Quality management system EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    13 Dec 2024
    Expires
    12 Dec 2029
  • EPT 0477.MDR.24/5669 Active

    Technical documentation EU MDR

    Certifier
    Eurofins Product Testing Italy S.r.l. 0477
    Issued
    13 Dec 2024
    Expires
    12 Dec 2029

Coverage

1 jurisdiction

Italy
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Italy

Specification

EUDAMED

Device Name
P.O.L. RX Crema, Pie Diabético
Model / Reference
420557 100 ml
Primary DI / UDI-DI
08032715360010
Basic UDI-DI
3271536123PN9
EMDN Code
V9099 Various devices not included in other classes - other
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000028381

Other devices from Difa Cooper S.p.A.

Properties

  • Animal Tissues

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No