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Proctoliz Med, MaxProctoliz Med, ProctoRapid, Proctoglid rectal cream

by Look Ahead SRL

Ref PO g25, PO g45

Active European Union

CE MDD

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/MDD NumberB-PO_gTE Basic UDI-DI D-PO_gTEUDI-DIDate30 Jun 2025RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Proctoliz med rectal gel
Model / Reference
PO g25, PO g45
Primary DI / UDI-DI
D-PO_gTE
Basic UDI-DI
B-PO_gTE
EMDN Code
G05 Topical anorectal administered gastro-intestinal system devices
Device Class
Class I
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
RO-MF-000001948

Other devices from Look Ahead SRL

Properties

Other properties (11)

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