Primary Device ID | 00862314000363 |
NIH Device Record Key | 212d784f-f34b-436f-a523-35ce13b2d07e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Johnson-Promident |
Version Model Number | UI-T330 |
Company DUNS | 965230188 |
Company Name | JOHNSON-PROMIDENT |
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 | false |
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 | 00862314000363 [Primary] |
ELC | Scaler, Ultrasonic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00862314000363]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-09-06 |
00862314000394 | ultrasonic scaling insert |
00862314000387 | ultrasonic scaling insert |
00862314000370 | ultrasonic scaling insert |
00862314000363 | ultrasonic scaling insert |
00862314000356 | ultrasonic scaling insert |
00862314000349 | ultrasonic scaling insert |
00862314000332 | ultrasonic scaling insert |
00862314000325 | ultrasonic scaling insert |
00862314000318 | ultrasonic scaling insert |