Primary Device ID | 07640163050028 |
NIH Device Record Key | 28e9dbd9-82f7-4062-ac7e-6d8189efd0b5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | inspiro Master Kit Syringe |
Version Model Number | 3020 |
Company DUNS | 486793370 |
Company Name | EDELWEISS DR ag |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640163050028 [Primary] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-10-12 |
07640163050011 - inspiro Master Kit Compule | 2018-03-29 inspiro Master Kit Compule |
07640163050028 - inspiro Master Kit Syringe | 2018-03-29inspiro Master Kit Syringe |
07640163050028 - inspiro Master Kit Syringe | 2018-03-29 inspiro Master Kit Syringe |
07640163050035 - inspiro Intro Kit Compule | 2018-03-29 inspiro Intro Kit Compule |
07640163050042 - inspiro Intro Kit Syringe | 2018-03-29 inspiro Intro Kit Syringe |
07640163050059 - inspiro Mini Kit Esthetic Anterior | 2018-03-29 inspiro Mini Kit Esthetic Anterior |
07640163050066 - inspiro Mini Kit General | 2018-03-29 inspiro Mini Kit General |
07640163050080 - inspiro Effect Shade Ice | 2018-03-29 inspiro Effect Shade Ice |
07640163050097 - inspiro Compule Trial Kit | 2018-03-29 inspiro Compule Trial Kit |