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Nti

FDA UDI

Class I (US FDA UDI)

by NTI - Kahla GmbH Rotary Dental Instruments

Identity

Trade Name
NTI FDA UDI
Generic Name
Pin/post dental drill bit FDA UDI
Device Name
NTI Endo Root Facer 1.10mm FDA UDI
Model / Reference
W6330 FDA UDI
Description
NTI Endo Root Facer 1.10mm FDA UDI

Identifiers

Catalog Number
ERF-1.10 FDA UDI
Primary DI / UDI-DI
E310W63301 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Pin/post dental drill bit 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: Pin/post dental drill bit

Nti by NTI - Kahla GmbH Rotary Dental Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pin/post dental drill bit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9ff47a2-4e9a-4b9d-8db2-21ccca18b841 34 fields · synced Jun 1, 2026