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 |