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i-system Shouldered Abutment Analog

EUDAMED

Class I (EU MDR)

Ref I-SSAA5065Ref I-SSAA4065

by Novodent SA

Identity

Trade Name
i-system Shouldered Abutment Analog EUDAMED
Device Name
Bone Level Mini Fixture Lab Analog EUDAMED
Model / Reference
I-SSAA5065 EUDAMED
I-SSAA4065 EUDAMED

Identifiers

Primary DI / UDI-DI
07630188202076 EUDAMED
07630188202069 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-system Shouldered Abutment Analog 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 (2)

  • EUDAMED 887d695e-78fe-42e5-8092-23bad78b3a99 61 fields · synced Sep 18, 2026
  • EUDAMED c97e16ab-0fd6-45d1-9bdf-2f0e004f2536 61 fields · synced May 17, 2026