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Ti-oss®

EUDAMEDFDA UDI

Class III (EU MDR)

Ref 10-0210Model 05-0210

by Chiyewon Co., LTD.

Identity

Trade Name
Ti-oss® EUDAMED
TI-OSS FDA UDI
Generic Name
Dental bone matrix implant, animal-derived FDA UDI
Device Name
Ti-oss® EUDAMED
Model / Reference
05-0210 EUDAMED
10-0210 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08809490620130 EUDAMEDFDA UDI
Basic UDI-DI
B-08809490620130 EUDAMED
FDA Product Code
NPM FDA UDI
EMDN Code
Q010302 DENTAL GRAFT DEVICES EUDAMED
GMDN Term
Dental bone matrix implant, animal-derived FDA UDI

Classification

Device Class
Class III EUDAMED
Class II FDA UDI
Regulation Number
872.3930 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Ti-oss® by Chiyewon Co., LTD. — Class III — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 750e46d1-dfac-4be9-b8f9-f36afa0c25ae 61 fields · synced Jul 27, 2026
  • FDA UDI 77fb9aad-a869-4a54-9ff3-4dc43ba428ef 32 fields · synced May 30, 2026