Primary Device ID | 00851640007122 |
NIH Device Record Key | f3bcae4b-0c29-4d01-821e-865ffddf7c7a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TrueStim |
Version Model Number | JQ-5C-J |
Company DUNS | 124034476 |
Company Name | Hi-Dow International Incorporated |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851640007122 [Primary] |
NGX | Stimulator, Muscle, Powered, For Muscle Conditioning |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 6 |
Public Version Date | 2019-10-28 |
Device Publish Date | 2016-09-01 |
00851640007429 | TrueStim Premium Stimulation System |
00851640007207 | TrueStim Premium Stimulation System 6-12 |
00851640007139 | Wired Classic Stimulation System BLACK |
00851640007122 | Wired Classic Stimulation System WHITE |
00851640007900 | Pulsed Electromagnetic Field Wrap,,LUMBAR WRAP Black |
00851640007931 | Pulsed Electromagnetic Field Wrap Black Neck Wrap |
00851640007917 | Pulsed Electromagnetic Field Wrap, Black, Knee Wrap |
00851640007924 | Pulsed Electromagnetic Field Wrap,,SHOULDER WRAP Black |
00081009308007 | Pulsed Electromagnetic Field Wrap, Black, lower limb wrap |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TRUESTIM 87063843 5173121 Live/Registered |
HI-DOW INTERNATIONAL, INC. 2016-06-08 |