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i-DAM

by UAB Medicinos linija 4 variants

Part of a family of 7 devices: see the family page

Ref IDABS

i-DAM (IDABS) is a Class I device made by UAB Medicinos linija, registered in EUDAMED on 29 Apr 2024 (Basic UDI-DI 4772178ML15LCLCUX), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4772178ML15LCLCUX Basic UDI-DI 04772178007643UDI-DIDate29 Apr 2024RegisteredStatusActive

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  • Withdrawn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
Light Curing Liquid Cofferdam
Model / reference
IDABS
Primary DI / UDI-DI
04772178007643
Basic UDI-DI
4772178ML15LCLCUX
EMDN code
Q0199 Odontology devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
LT-MF-000002719

Similar devices in this category

Other devices filed under ODONTOLOGY DEVICES - OTHER.

Other devices from UAB Medicinos linija

See all devices from UAB Medicinos linija →

Properties

Other properties (14, all answered No)