← Back to catalogue

Ti Abutment Screw

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref ASR200

by OSSTEM IMPLANT Co., Ltd.

Identity

Trade Name
Ti Abutment Screw EUDAMED
US System FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Dental Abutment System EUDAMED
Model / Reference
ASR200 EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
08800000910475 EUDAMEDFDA UDI
Basic UDI-DI
88000406ABUTMENTRZ EUDAMED
510(k) Number
K062030 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Czechia EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

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

No

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

Ti Abutment Screw by Osstem Implant Co., Ltd. — Class IIb — 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 (2)

  • EUDAMED 87036bda-b0ba-4935-b6df-c1091b2c9cea 61 fields · synced Jun 19, 2026
  • FDA UDI 43c93c43-c84d-42fc-8e07-6750336ab14d 33 fields · synced May 30, 2026