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Keraring

by Mediphacos Industrias Médicas S/A 341 variants

Ref SI6A340M250Model SI6-340° 250µ

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07899330018020 Basic UDI-DI 07899330018020UDI-DIDate17 Mar 2023RegisteredStatusActive

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  • Withdrawn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 SI6-340° 250µ
Model / Reference
SI6-340° 250µ, SI6A340M250
Primary DI / UDI-DI
07899330018020
Basic UDI-DI
B-07899330018020
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

  • Sterile
  • Implantable

Other properties (9)

  • 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