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Keraring

by Mediphacos Industrias Médicas S/A 341 variants

Ref SI6A125M300Model SI6-125° 300µ

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 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/MDD NumberB-07899330096967 Basic UDI-DI 07899330096967UDI-DIDate17 Feb 2022RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Keraring SI6-125° 300µ
Model / Reference
SI6-125° 300µ, SI6A125M300
Primary DI / UDI-DI
07899330096967
Basic UDI-DI
B-07899330096967
EMDN Code
P0399 Ocular prostheses - other
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
BR-MF-000015743
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Mediphacos Industrias Médicas S/A

See all devices from Mediphacos Industrias Médicas S/A →

Properties

  • Implantable
  • Contains Latex

Other properties (9)

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