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iO bone Syringe

EUDAMED

Class III (EU MDR)

Ref S05-0210

by Chiyewon Co., LTD.

Identity

Trade Name
iO bone Syringe EUDAMED
Device Name
iO bone Syringe EUDAMED
Model / Reference
S05-0210 EUDAMED

Identifiers

Primary DI / UDI-DI
08809490624251 EUDAMED
Basic UDI-DI
B-08809490624251 EUDAMED
EMDN Code
Q010302 DENTAL GRAFT DEVICES EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Italy 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

Yes

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

iO bone Syringe by Chiyewon Co., LTD. — Class III — 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

Manufacturer
Chiyewon Co., LTD.
EUDAMED SRN
KR-MF-000022264
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 28f3581c-7822-41f4-88f9-5e48f972f28b 61 fields · synced Jun 19, 2026