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Drill extension

FDA UDI

Class I (US FDA UDI)

by Thommen Medical AG

Identity

Trade Name
Drill extension FDA UDI
Generic Name
Dental drill bit extension FDA UDI
Model / Reference
3.03.231 FDA UDI

Identifiers

Primary DI / UDI-DI
07640156475326 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental drill bit extension FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental drill bit extension

Drill extension by Thommen Medical AG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental drill bit extension.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thommen Medical AG

Sources (1)

  • FDA UDI 6508fc95-317b-49d7-b9c0-f1913d8b6bd1 32 fields · synced Jun 8, 2026