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I-LiNQ Impression Post

EUDAMED

Class I (EU MDR)

Ref I-SILIP65

by Novodent SA

Identity

Trade Name
I-LiNQ Impression Post EUDAMED
Device Name
Bone Level Mini Fixture Lab Analog EUDAMED
Model / Reference
I-SILIP65 EUDAMED

Identifiers

Primary DI / UDI-DI
07630188204810 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 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

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Manufacturer

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

Sources (1)

  • EUDAMED e55fae2b-6797-46ef-ae01-a5c432488e5e 61 fields · synced Jul 13, 2026