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S3810

EUDAMED

Class IIb (EU MDR)

Ref S3810

by I Do Biotech Co., Ltd

Identity

Trade Name
S3810 EUDAMED
Device Name
Fixture EUDAMED
Model / Reference
S3810 EUDAMED

Identifiers

Primary DI / UDI-DI
08800075210906 EUDAMED
Basic UDI-DI
B-08800075210906 EUDAMED
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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

S3810 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 400487e2-84dc-4272-ac97-dd7da98120dc 61 fields · synced Jul 28, 2026