| Primary Device ID | 07640163050097 |
| NIH Device Record Key | f0e65dfc-0bc3-42eb-8b2a-de1356b0ba34 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | inspiro Compule Trial Kit |
| Version Model Number | 3070 |
| 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 | 07640163050097 [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 | 2016-10-19 |
| 07640163050011 - inspiro Master Kit Compule | 2018-03-29 inspiro Master Kit Compule |
| 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 | 2018-03-29inspiro Compule Trial Kit |
| 07640163050097 - inspiro Compule Trial Kit | 2018-03-29 inspiro Compule Trial Kit |