| Primary Device ID | 40827160110107 |
| NIH Device Record Key | 9ab6d30e-9aed-4145-8fe7-846308f3c94f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | pjur Aqua |
| Version Model Number | pjur Aqua 500 ml - USA |
| Company DUNS | 400744553 |
| Company Name | Pjur Group Luxembourg SA |
| 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 | 00827160110109 [Primary] |
| GS1 | 10827160110106 [Package] Contains: 00827160110109 Package: pack [2 Units] In Commercial Distribution |
| GS1 | 40827160110107 [Package] Contains: 10827160110106 Package: case [15 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 | 2019-01-04 |
| Device Publish Date | 2018-12-04 |
| 40827160110107 | Water-based Personal Lubricant |
| 40827160110091 | Water-based Personal Lubricant |
| 40827160110084 | Water-based Personal Lubricant |
| 40827160100252 | Water-based Personal Lubricant |