Ti-Max X

GUDID 04560264510906

NAKANISHI INC.

Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary Dental power tool converter attachment, non-rotary

Primary Device ID	04560264510906
NIH Device Record Key	5f18a8c3-227e-41ef-82f6-f25db32f97d3
Commercial Distribution Discontinuation	2021-02-15
Commercial Distribution Status	In Commercial Distribution
Brand Name	Ti-Max X
Version Model Number	X55
Company DUNS	690710546
Company Name	NAKANISHI INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04560264510906 [Primary]

FDA Product Code

EGS	Handpiece, contra- and right-angle attachment, dental