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Non-Sterile Dental Abutment

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref MUS-9151Model ScrewModel Impression Coping – Transfer

by Ditron Dental Ltd.

Identity

Trade Name
Non-Sterile Dental Abutment EUDAMED
Impression Coping – Transfer EUDAMED
Ditron Dental FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Open Tray Screw for Multi-Unit Abutment Short EUDAMED
Abutment Impression Close Tray Transfer EUDAMED
Closed Tray Screw for Multi-Unit Abutment FDA UDI
Model / Reference
Screw EUDAMED
MUS-9151 EUDAMEDFDA UDI
Impression Coping – Transfer EUDAMED
Description
Closed Tray Screw for Multi-Unit Abutment FDA UDI

Identifiers

Catalog Number
MUS-9151 FDA UDI
Primary DI / UDI-DI
07290109282992 EUDAMEDFDA UDI
Basic UDI-DI
B-07290109282992 EUDAMED
729010928TRANGA EUDAMED
Direct Marketing DI
07290109282992 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
Q010599 DENTAL INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

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

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Non-Sterile Dental Abutment by Ditron Dental Ltd — Class IIb — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ditron Dental Ltd.
EUDAMED SRN
IL-MF-000015966
Authorised Representative
MedNet EC-REP IIb GmbH DE-AR-000011192

Sources (3)

  • EUDAMED ba12e750-7048-42cb-9904-6b6612953def 61 fields · synced Jun 19, 2026
  • FDA UDI 837c6cce-809b-4608-83c4-6f703df6aca2 35 fields · synced May 30, 2026
  • EUDAMED 65d8bc35-561a-4244-8361-870ef9ed1d78 61 fields · synced Jun 19, 2026