| Primary Device ID | 00852930006313 |
| NIH Device Record Key | 7a7dad4e-1dc8-456a-b87e-2dee5676f19d |
| Commercial Distribution Discontinuation | 2022-12-31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DRYBUDDY |
| Version Model Number | DBFL3 |
| Catalog Number | DBFL3 |
| Company DUNS | 932984375 |
| Company Name | ENURESIS SOLUTIONS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00852930006313 [Primary] |
| KPN | Alarm, Conditioned Response Enuresis |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-17 |
| Device Publish Date | 2019-04-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() DRYBUDDY 76552191 3411905 Live/Registered |
ENURESIS SOLUTIONS LLC 2003-10-17 |