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My Filler Strong

by My Med Kft

Ref MYF003

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05999861845026 Basic UDI-DI 05999861845026UDI-DIDate15 Sep 2026RegisteredStatusActive

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

SwedenLithuaniaGermanyFranceSlovakiaHungaryRomaniaSpainItalyTürkiyeCroatiaGreeceCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • Croatia
  • Cyprus
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Lithuania
  • Romania
  • Slovakia
  • Spain
  • Sweden
  • Türkiye

Specification

EUDAMED

Model / Reference
MYF003
Primary DI / UDI-DI
05999861845026
Basic UDI-DI
B-05999861845026
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
HU-MF-000028567

Other devices from My Med Kft

See all devices from My Med Kft →

Properties

  • Sterile

Other properties (10)

  • 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