Primary Device ID | 00851640007474 |
NIH Device Record Key | 50729442-8eb4-4aaa-a8f0-dad16a9fa8e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hi-Dow |
Version Model Number | JQ-5C-T |
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 | 00851640007474 [Primary] |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-28 |
Device Publish Date | 2018-07-19 |
00851640007474 | Wired Electronic Muscle Stimulator , XPDS-4-24 |
00851640007399 | Wireless-49 TENS/EMS System |
00851640007016 | AcuXP iSmart Black |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HI-DOW 98091715 not registered Live/Pending |
Hi-Dow IPHC, Inc. 2023-07-19 |
HI-DOW 77826539 3784054 Live/Registered |
Hi-Dow International 2009-09-15 |