Primary Device ID | 40827160114211 |
NIH Device Record Key | 37b0fb29-5293-4536-8b3c-bff6efe1ac92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arcwave by pjur |
Version Model Number | Arcwave by pjur 10ml |
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 | 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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00827160114213 [Primary] |
GS1 | 10827160114210 [Package] Contains: 00827160114213 Package: pack [50 Units] In Commercial Distribution |
GS1 | 40827160114211 [Package] Contains: 10827160114210 Package: case [500 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 | 2020-01-16 |
Device Publish Date | 2020-01-08 |
40827160114211 | Water-based Personal Lubricant |
10827160114739 | Water-based Personal Lubricant |