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Multi Unit Abutment Impression Pick-up Screw

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MUAIPS48

by Neobiotech Co., Ltd.

Identity

Trade Name
Multi Unit Abutment Impression Pick-up Screw EUDAMED
Neobiotech Implant System FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Dental Surgical Instrument EUDAMED
ø2.3 FDA UDI
Model / Reference
MUAIPS48 EUDAMEDFDA UDI
Description
ø2.3 FDA UDI

Identifiers

Primary DI / UDI-DI
08809876900160 EUDAMEDFDA UDI
Basic UDI-DI
880927676NBRSIRSCL1S03FT EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Poland 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

Multi Unit Abutment Impression Pick-up Screw by Neobiotech 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

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Manufacturer

EUDAMED SRN
KR-MF-000016946
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (2)

  • EUDAMED 51b29f92-a69f-490a-8393-b40c8352b6f0 61 fields · synced Jul 9, 2026
  • FDA UDI 0d793a82-0d8d-4175-b852-c0d402c32730 33 fields · synced May 29, 2026