← Back to catalogue

Ditron Dental

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref DGS-TE100Model Guided Insertion Mount

by Ditron Dental Ltd

Identity

Trade Name
Tool Extractor EUDAMED
Ditron Dental FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Direct Insertion Mount EUDAMED
Tool Extractor FDA UDI
Model / Reference
DGS-TE100 EUDAMEDFDA UDI
Guided Insertion Mount EUDAMED
Description
Tool Extractor FDA UDI

Identifiers

Catalog Number
DGS-TE100 FDA UDI
Primary DI / UDI-DI
07290109284538 EUDAMEDFDA UDI
Basic UDI-DI
729010928MOUNG6 EUDAMED
Direct Marketing DI
07290109284538 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - 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

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

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

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

Manufacturer

Manufacturer
Ditron Dental Ltd

Sources (2)

  • FDA UDI 63f40c93-6f84-4eb7-a2a0-9dc84ea9dbbf 35 fields · synced Aug 5, 2026
  • EUDAMED 4aa8efe4-7b41-4fe9-abd4-ee9ff64755d1 61 fields · synced Aug 5, 2026