← Back to catalogue

Snucone Implant System

EUDAMED

Class IIb (EU MDR)

Ref AF+B-3512

by Snucone Co., Ltd.

Identity

Trade Name
Snucone Implant System EUDAMED
Device Name
Abiding Fixture+B (AF+B) EUDAMED
Model / Reference
AF+B-3512 EUDAMED

Identifiers

Primary DI / UDI-DI
08800020800404 EUDAMED
Basic UDI-DI
B-08800020800404 EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Snucone Implant System by SNUCONE Co., LTD. — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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

Manufacturer

Manufacturer
Snucone Co., Ltd.
EUDAMED SRN
KR-MF-000036358
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 2957cce3-b22c-4469-9e5f-48264f42b0f4 61 fields · synced May 23, 2026