← Back to catalogue

i-LiNQ Conometric Impression Post

EUDAMED

Class I (EU MDR)

Ref I-SILCONOIP50Ref I-SILCONOIP65

by Novodent SA

Identity

Trade Name
i-LiNQ Conometric Impression Post EUDAMED
Device Name
Bone Level Mini Fixture Lab Analog EUDAMED
Model / Reference
I-SILCONOIP50 EUDAMED
I-SILCONOIP65 EUDAMED

Identifiers

Primary DI / UDI-DI
07630188204933 EUDAMED
07630188204940 EUDAMED
Basic UDI-DI
764016818003D7 EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

i-LiNQ Conometric Impression Post by Novodent SA — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Novodent SA
EUDAMED SRN
CH-MF-000023309
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 249db15c-5efe-4c8e-9035-417e035f2664 61 fields · synced Jul 17, 2026
  • EUDAMED b6979781-82e5-4fe9-b40d-9e0f02af0544 61 fields · synced May 17, 2026