Lime K Kent Dental

by Conception Et Fabrication De Produits Medicaux Et Paramedicaux 36 variants

Ref 3168466Model Instruments endodontiques manuels

Active European Union

CE MDR

Valid until

Not listed

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

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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number3665318BLR004NV Basic UDI-DI 03665318028701UDI-DI	Date22 Jul 2026Registered	StatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Lime K
Model / Reference: Instruments endodontiques manuels, 3168466

Primary DI / UDI-DI: 03665318028701
Basic UDI-DI: 3665318BLR004NV
EMDN Code: Q010507 Endodontic instruments (canal enlargers, files, rasps, etc.), single-use

Device Class: Class I
EU market of registration: France

Manufacturer details

EUDAMED SRN: FR-MF-000010345

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Properties

Other properties (13)

Sterile: No
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