← Back to catalogue

Bone Tack Holder

EUDAMEDFDA UDI

Class I (EU MDR)

Ref OBTHRef HOBTH

by OSSTEM IMPLANT Co., Ltd.

Identity

Trade Name
Bone Tack Holder EUDAMEDFDA UDI
Generic Name
Manual non-rotary dental instrument handle FDA UDI
Device Name
Surgical Instrument System EUDAMED
Model / Reference
OBTH EUDAMEDFDA UDI
HOBTH EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800121707183 EUDAMED
08800121777001 EUDAMEDFDA UDI
08800209368824 EUDAMEDFDA UDI
Basic UDI-DI
88000406CLASSIBS25V EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Manual non-rotary dental instrument handle FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Czechia EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Bone Tack Holder by Osstem Implant Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (5)

  • EUDAMED 8f3a4816-0ca4-4821-be2c-6facdf086616 61 fields · synced Jul 22, 2026
  • FDA UDI 148a9e09-77ed-455a-b7ac-6434ba324d53 32 fields · synced May 30, 2026
  • FDA UDI 580110a1-ac47-432e-959c-ba45c5b29698 32 fields · synced May 30, 2026
  • EUDAMED 229e22a8-fce5-4dd2-8f6b-b35154c68ec0 61 fields · synced Jul 17, 2026
  • EUDAMED a82774c0-5a44-42ea-bf9e-53d19f6ac918 61 fields · synced Jul 22, 2026