| Primary Device ID | 00817051023472 |
| NIH Device Record Key | b986209c-2ca7-4d7f-843f-8df298cf77ee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Benda Brush |
| Version Model Number | 370101 |
| 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 | 00817051023472 [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 |
| 00817051023496 | Benda Brush Mini Red |
| 00817051023489 | Benda Brush Regular Blue |
| 00817051023472 | Benda Brush Regular Multi-colors |
| 00817051022635 | Benda Brush Mini Green |
| 00817051022628 | Benda Brush Mini Yellow |
| 00817051022611 | Benda Brush Mini Blue |
| 00817051022604 | Benda Brush Mini Red |
| 00817051022598 | Benda Brush Regular Green |
| 00817051022581 | Benda Brush Regular Yellow |
| 00817051022574 | Benda Brush Regular BLUE |
| 00817051022567 | Benda Brush Regular Red |