| Primary Device ID | 00702173151885 |
| NIH Device Record Key | 7d945ebf-095d-4170-89b7-64dbe7e820c9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Q-Sweat |
| Version Model Number | 5188 |
| Company DUNS | 006196604 |
| Company Name | WR MEDICAL ELECTRONICS CO 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 | true |
| 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 | false |
| Phone | 651-604-8400 |
| info@wrmed.com | |
| Phone | 651-604-8400 |
| info@wrmed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00702173151885 [Primary] |
| KTB | Device, Iontophoresis, Specific Uses |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-12 |
| 00702173122755 - Therabath | 2020-03-19 |
| 00702173122809 - Therabath | 2019-11-14 |
| 00702173139005 - Hilger Dual Stim | 2018-07-06 |
| 00702173139050 - Hilger Dual-Stimulator Remote Probe | 2018-07-06 |
| 00702173151885 - Q-Sweat | 2018-07-06 |
| 00702173151885 - Q-Sweat | 2018-07-06 |
| 00702173151915 - Meridian™ Iontophoretic Drug Delivery Electrode | 2018-07-06 |
| 00702173152929 - Meridian™ Iontophoretic Drug Delivery Electrode | 2018-07-06 |
| 00702173155920 - Iontophor®-II | 2018-07-06 |