Primary Device ID | 30688504003454 |
NIH Device Record Key | 20cb0883-32fc-46dc-aff7-56a3f83e2b2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Floravi |
Version Model Number | Silicone Lubricant |
Company DUNS | 879057065 |
Company Name | WESTRIDGE LABORATORIES INCORPORATED |
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 | false |
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 | false |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Total Volume | 4 Fluid Ounce |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00688504003453 [Primary] |
GS1 | 30688504003454 [Package] Contains: 00688504003453 Package: Case [12 Units] In Commercial Distribution |
NUC | Lubricant, Personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2017-07-19 |
00688504005402 | 1 oz Water Based Disc Cap Bottle |
30688504003461 | This is a water-based personal lubricant and is compatible with both Polyurethane and Latex Cond |
30688504003454 | A silicone lubricant that is latex compatible. |