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485 Kit

EUDAMED

Class IIa (EU MDR)

Ref H485K

by OSSTEM IMPLANT Co., Ltd.

Identity

Trade Name
485 KIT EUDAMED
Device Name
Surgical KIT System EUDAMED
Model / Reference
H485K EUDAMED

Identifiers

Primary DI / UDI-DI
08809917108548 EUDAMED
Basic UDI-DI
88000406DRILLKITSYSTEMD6 EUDAMED
EMDN Code
L159016 DENTAL SURGERY INSTRUMENT KITS, REUSABLE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

485 Kit by Osstem Implant Co., Ltd — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
KR-MF-000020006
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED f3681e53-670c-4728-bd48-0983aa3eba40 61 fields · synced Oct 6, 2026