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Linicin Plus Solution

by Oystershell NV 2 variants

Part of a family of 9 devices: see the family page

Ref 07010769Model X92001482

Linicin Plus Solution (07010769) is a Class I device made by Oystershell NV, registered in EUDAMED on 17 Oct 2025 (Basic UDI-DI 5410765ElimaxLotionHS), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5410765ElimaxLotionHS Basic UDI-DI 05410765004857UDI-DIDate17 Oct 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Elimax Lotion I
Model / reference
X92001482, 07010769
Primary DI / UDI-DI
05410765004857
Basic UDI-DI
5410765ElimaxLotionHS
EMDN code
V901001 Lice elimination mechanical devices
Device class
Class I
EU registration type
Standard device
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
BE-MF-000011797

Similar devices in this category

Other devices filed under LICE ELIMINATION MECHANICAL DEVICES.

Other devices from Oystershell NV

See all devices from Oystershell NV →

Properties

Other properties (14, all answered No)