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rootEX drill short shank 1, 6 mm, pu: 6

FDA UDI

Class I (US FDA UDI)

by Diaswiss SA

Identity

Trade Name
rootEX drill short shank 1,6 mm, pu: 6 FDA UDI
Generic Name
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI
Device Name
Rotary instrument for endodontic intraoral use FDA UDI
Model / Reference
935K.016med FDA UDI
Description
Rotary instrument for endodontic intraoral use FDA UDI

Identifiers

Primary DI / UDI-DI
07630049952614 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Rotary/reciprocating endodontic file/rasp, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rotary/reciprocating endodontic file/rasp, reusable

rootEX drill short shank 1, 6 mm, pu: 6 by Diaswiss SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rotary/reciprocating endodontic file/rasp, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Diaswiss SA

Sources (1)

  • FDA UDI 44e07106-39ed-40d2-9e00-539cbddbd69c 33 fields · synced May 30, 2026