Primary Device ID | 04560264560079 |
NIH Device Record Key | 38954b86-9208-4464-b8b0-88dbc9c74067 |
Commercial Distribution Discontinuation | 2018-07-11 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Ti-Max X |
Version Model Number | X-SG20L |
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 Issuing Agency | Device ID |
---|---|
GS1 | 04560264560079 [Primary] |
KMW | HANDPIECE, ROTARY BONE CUTTING |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04560264560079]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-22 |
Device Publish Date | 2016-09-16 |
04560264560673 | X-SG65 |
04560264560529 | X-SG65L |
04560264560253 | X-DSG20 |
04560264560246 | X-DSG20L |
04560264560192 | X-SG25L |
04560264560185 | X-SG93 |
04560264560086 | X-SG93L |
04560264560079 | X-SG20L |
04560264557093 | X-SG20L |
04560264533257 | X-SG65 |
04560264528499 | X-DSG20Lh |
04560264528482 | X-DSG20h |
04560264528475 | X-DSG20L |
04560264528468 | X-DSG20 |
04560264518575 | X-SG65L |
04560264518513 | X-SG25L |
04560264517912 | X-SG93 |
04560264517905 | X-SG93L |
04560264516953 | X-SG20L |
04560264516878 | X500KL |
04560264510906 | X55 |
04560264510890 | X55L |
04560224993183 | X500KL |
04560224993138 | X500L |
04560264530768 | X95EX |
04560264510944 | X35 |
04560264510937 | X35L |
04560264510920 | X57 |
04560264510913 | X57L |
04560264523692 | X600WLED |