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Ditron Dental

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref ITDS-300290Model Prosthetic Screwdrivers

by Ditron Dental Ltd

Identity

Trade Name
Insertion Drivers EUDAMED
Ditron Dental FDA UDI
Generic Name
Dental/maxillofacial surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Angulated Prosthetic Screwdriver, WL15mm L27mm EUDAMED
CC Sort Implant Torque Driver Hex 2.0 FDA UDI
Model / Reference
ITDS-300290 EUDAMEDFDA UDI
Prosthetic Screwdrivers EUDAMED
Description
CC Sort Implant Torque Driver Hex 2.0 FDA UDI

Identifiers

Catalog Number
ITDS-300290 FDA UDI
Primary DI / UDI-DI
07290109284835 EUDAMEDFDA UDI
Basic UDI-DI
729010928DRIVE2 EUDAMED
Direct Marketing DI
07290109284835 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

Yes

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 b744e536-0773-4644-9ca2-3221173b456c 35 fields · synced Jun 19, 2026
  • EUDAMED a0219dbd-071d-4217-b68a-ca625d63a6cc 61 fields · synced Jun 19, 2026