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Kit Mini Well Proxa Toric +17.0SE CL2.5

by SIFI S.p.A.

Ref 1131CCZ

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 linked in EUDAMED

A group certificate may exist

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 Number8027864SIFIMDF35NE Basic UDI-DI 08027864094329UDI-DIDate20 Feb 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
MINI WELL TORIC (KIT) and MINI WELL PROXA TORIC (KIT)
Model / Reference
1131CCZ
Primary DI / UDI-DI
08027864094329
Basic UDI-DI
8027864SIFIMDF35NE
EMDN Code
P030102100302 IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHILIC ACRYLIC
Device Class
Class IIb
Medical Purpose
MINI WELL TORIC and MINI WELL PROXA TORIC intraocular lenses are intended for primary implantation for visual correction of aphakia and pre-existing corneal astigmatism in adults with or without presbyopia after removal of a cataractous lens and aphakia after lensectomy in presbyopic adults with corneal astigmatism who desire increased spectacle independence for distance and near vision.

Manufacturer details

EUDAMED SRN
IT-PR-000021264

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Properties

  • Sterile