Primary Device ID | 10843445043990 |
NIH Device Record Key | 8f51c993-1303-482d-a090-27b932dac4b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | hydrolube, personal lubricant, 4 oz. |
Version Model Number | 6707 |
Company DUNS | 128889172 |
Company Name | Beacon Wellness Brands |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00843445056627 [Primary] |
GS1 | 00843445056672 [Package] Package: Master Carton [6 Units] In Commercial Distribution |
GS1 | 10843445043990 [Package] Contains: 00843445056627 Package: INNER CARTON [6 Units] In Commercial Distribution |
NUC | Lubricant, Personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-21 |
Device Publish Date | 2023-12-13 |