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Ditron Dental

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref MUP-9140Model Impression Coping – Transfer

by Ditron Dental Ltd

Identity

Trade Name
Impression Coping – Transfer EUDAMED
Ditron Dental FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Abutment Impression Close Tray Transfer EUDAMED
Closed Tray Transfer for Multi-Unit Abutment FDA UDI
Model / Reference
MUP-9140 EUDAMEDFDA UDI
Impression Coping – Transfer EUDAMED
Description
Closed Tray Transfer for Multi-Unit Abutment FDA UDI

Identifiers

Catalog Number
MUP-9140 FDA UDI
Primary DI / UDI-DI
07290109282930 EUDAMEDFDA UDI
Basic UDI-DI
729010928TRANGA EUDAMED
Direct Marketing DI
07290109282930 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010599 DENTAL INSTRUMENTS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
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

Category: Dental/maxillofacial surgical procedure kit, non-medicated, reusable

Ditron Dental by Ditron Dental Ltd — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental/maxillofacial surgical procedure kit, non-medicated, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ditron Dental Ltd

Sources (2)

  • FDA UDI 112a4b9b-9a86-4a71-8c19-377d76022c8b 35 fields · synced Jun 19, 2026
  • EUDAMED 55dd7ffd-cf50-465b-999e-d33c27280cc6 61 fields · synced Jun 19, 2026