| Primary Device ID | 00188813000247 |
| NIH Device Record Key | 88055dfc-cfd8-481a-a02f-1c9383a59617 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Wet-Stop |
| Version Model Number | WS103 |
| Company DUNS | 146730481 |
| Company Name | POTTYMD, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00188813000247 [Primary] |
| KPN | Alarm, Conditioned Response Enuresis |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-01-08 |
| Device Publish Date | 2017-02-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() WET-STOP 97613576 not registered Live/Pending |
POTTYMD, LLC 2022-09-29 |
![]() WET-STOP 73770302 1556640 Live/Registered |
LEVIN, PAUL D. 1988-12-19 |