| Primary Device ID | E22121921 |
| NIH Device Record Key | 82d20057-c110-413b-b480-361bba8e0d94 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mixing tips |
| Version Model Number | 2192 |
| Company DUNS | 316699578 |
| Company Name | VOCO GmbH |
| Device Count | 50 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | 999-999-9999 |
| xxx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | E2212192 [Unit of Use] |
| HIBCC | E22121921 [Primary] |
| EID | Syringe, Restorative And Impression Material |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-04-11 |
| Device Publish Date | 2019-04-03 |
| E22121961 | Mixing tips type 16 |
| E22121951 | Mixing tips type 15 |
| E22121941 | Mixing tips type 14 |
| E22121931 | Mixing tips type 13 |
| E22121921 | Mixing tips type 12 |
| E22121911 | Mixing tips type 11 |
| E2212191 | Mixing tips type 19 |
| E22121891 | Mixing tips type 10 |
| E22121881 | Mixing tips type 9 |
| E22121871 | Mixing tips type 8 |
| E22122021 | Mixing tips type 20 |
| E22121851 | Mixing tips type 6 |
| E22122031 | Mixing tips type 30 |
| E22121861 | Mixing tips type 7 |
| E22122040 | Mixing tips type 31 |