| Primary Device ID | 00817051022673 |
| NIH Device Record Key | dac1a957-b745-487f-b8ab-ac37887aea2e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Benda Micro |
| Version Model Number | 380013 |
| Company DUNS | 053707303 |
| Company Name | CENTRIX, INC. |
| Device Count | 1 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817051022673 [Primary] |
| KXR | Applicator, Resin |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-08 |
| Device Publish Date | 2023-12-29 |
| 00817051023502 | Benda Micro Fine Red |
| 00817051022819 | Benda Micro X-fine Assorted |
| 00817051022796 | Benda Micro X-fine Ivory |
| 00817051022772 | Benda Micro Twin Light Green |
| 00817051022765 | Benda Micro Twin Ivory |
| 00817051022758 | Benda Micro Twin Blue |
| 00817051022741 | Benda Micro Twin Pink |
| 00817051022734 | Benda Micro Twin Blue |
| 00817051022727 | Benda Micro Twin Pink |
| 00817051022710 | Benda Micro Regular Silver |
| 00817051022703 | Benda Micro Regular Purple |
| 00817051022697 | Benda Micro Regular Green |
| 00817051022680 | Benda Micro Regular Blue |
| 00817051022673 | Benda Micro Fine Red |
| 00817051022659 | Benda Micro Fine Assorted |
| 00817051022642 | Benda Micro Regular Assorted |