Primary Device ID | 40827160110091 |
NIH Device Record Key | ae711f80-e67d-48db-850a-da3855cfa086 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | pjur Aqua |
Version Model Number | pjur Aqua 250 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 | 00827160110093 [Primary] |
GS1 | 10827160110090 [Package] Contains: 00827160110093 Package: pack [4 Units] In Commercial Distribution |
GS1 | 40827160110091 [Package] Contains: 10827160110090 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 | 4 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2017-01-25 |
40827160110107 | Water-based Personal Lubricant |
40827160110091 | Water-based Personal Lubricant |
40827160110084 | Water-based Personal Lubricant |
40827160100252 | Water-based Personal Lubricant |