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 |