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LENSCARE KOMBI-GEL-SYSTEM 380 ml - only bottle (standard label)

by Esoform S.p.A.

Ref P10406LHLFJModel Soluzioni per cura di LAC

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-08057149553838 Basic UDI-DI 08057149553838UDI-DIDate9 Oct 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

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Lensea GP 200ml (60)
Model / Reference
Soluzioni per cura di LAC, P10406LHLFJ
Primary DI / UDI-DI
08057149553838
Basic UDI-DI
B-08057149553838
EMDN Code
Q02030204 Contact lenses storing and cleaning solutions
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000028984

Other devices from Esoform S.p.A.

See all devices from Esoform S.p.A. →

Properties

  • Sterile

Other properties (12)

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