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Ditron Dental

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref TRAL-200240Model Prosthetic Screwdrivers

by Ditron Dental Ltd

Identity

Trade Name
Prosthetic Screwdrivers EUDAMED
Ditron Dental FDA UDI
Generic Name
Surgical screwdriver, reusable FDA UDI
Device Name
Angulated Prosthetic Screwdriver, WL15mm L27mm EUDAMED
Long Ratchet Screwdriver Hex 1.25 FDA UDI
Model / Reference
TRAL-200240 EUDAMEDFDA UDI
Prosthetic Screwdrivers EUDAMED
Description
Long Ratchet Screwdriver Hex 1.25 FDA UDI

Identifiers

Catalog Number
TRAL-200240 FDA UDI
Primary DI / UDI-DI
07290109285764 EUDAMEDFDA UDI
Basic UDI-DI
729010928DRIVE2 EUDAMED
Direct Marketing DI
07290109285764 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
L159099 ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Surgical screwdriver, 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: Surgical screwdriver, 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 Surgical screwdriver, 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 68ca38d2-5f3e-420d-ad02-b94180001cbc 35 fields · synced Jun 19, 2026
  • EUDAMED 502bf368-39a6-42cc-b20d-1a0c030d76fa 61 fields · synced Jun 14, 2026