Primary Device ID | 80023601680064 |
NIH Device Record Key | bc6ce738-0ea4-4eef-9694-3ca0d3e52a75 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TENS 7000 |
Version Model Number | DT7202-48 |
Company DUNS | 827221698 |
Company Name | COMPASS HEALTH BRANDS CORP. |
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 | true |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00023601680068 [Primary] |
GS1 | 80023601680064 [Package] Contains: 00023601680068 Package: [20 Units] In Commercial Distribution |
NUH | Stimulator, Nerve, Transcutaneous, Over-The-Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-06 |
Device Publish Date | 2024-10-29 |
00092237622162 | Tens 7000 OTC Electrodes, White Cloth, Mixed 32/pk Includes (16) 2" x 2" square electrodes and |
00092237624555 | TENS 7000 Rechargeable 4 Channel DDX |
00092237624548 | TENS 7000 Rechargeable + EMS DDX |
00092237624531 | TENS 7000 Rechargeable DDX |
30092237626642 | TENS 7000 Menstrual TENS |
80023601680378 | TENS 7000 w 16 pk |
80023601680064 | TENS 7000 w 48 pk |
30092237626659 | TENS 7000 Migraine TENS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
TENS 7000 85372176 4134482 Live/Registered |
COMPASS HEALTH BRANDS CORP. 2011-07-15 |