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Final Abutment

EUDAMED

Class IIb (EU MDR)

Ref MSL6052

by I Do Biotech Co., Ltd

Identity

Device Name
Final Abutment EUDAMED
Model / Reference
MSL6052 EUDAMED

Identifiers

Primary DI / UDI-DI
08800075205346 EUDAMED
Basic UDI-DI
B-08800075205346 EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Final Abutment by I Do Biotech 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

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Manufacturer

EUDAMED SRN
KR-MF-000022539
Authorised Representative
Valdent S.L. ES-AR-000022075

Sources (1)

  • EUDAMED b0d0989b-70ab-4744-9689-02600606e2b1 61 fields · synced Jun 20, 2026