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UF(II) Internal Hybrid Link

EUDAMED

Class IIb (EU MDR)

Ref DIO Implant System Product Catalog Ver 7.0 (KR)Model SIHL 50401O[H]

by DIO Corporation

Identity

Trade Name
UF(II) Internal Hybrid Link EUDAMED
Device Name
UF(II) Internal Hybrid Link EUDAMED
Model / Reference
SIHL 50401O[H] EUDAMED
DIO Implant System Product Catalog Ver 7.0 (KR) EUDAMED

Identifiers

Primary DI / UDI-DI
08800049423585 EUDAMED
Basic UDI-DI
880004925008BE EUDAMED
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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

UF(II) Internal Hybrid Link by DIO Corporation — Class IIb — 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
DIO Corporation
EUDAMED SRN
KR-MF-000008515
Authorised Representative
AR Experts B.V. NL-AR-000023989

Sources (1)

  • EUDAMED df22ae55-6ab6-4209-a1af-9b7381a6bf93 61 fields · synced Aug 1, 2026