| Primary Device ID | 04719873120666 |
| NIH Device Record Key | 14e58fa3-a6a4-4e15-910c-49ad6a4f4441 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 20:1 CONTRA ANGLE |
| Version Model Number | LCC-120A |
| Company DUNS | 657263687 |
| Company Name | BONART CO., LTD. |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| 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 | 04719873120666 [Primary] |
| EGS | Handpiece, Contra- And Right-Angle Attachment, Dental |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[04719873120666]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-12-13 |
| Device Publish Date | 2018-11-12 |
| 04719873121533 - ART TRIPLE BEND 25kHz | 2023-04-03 |
| 04719873121540 - ART TRIPLE BEND 30kHz | 2023-04-03 |
| 04719873121410 - PIEZO TIP/BE-P | 2022-03-28 |
| 04719873121366 - 25K FS-SLIM PLASTIC INSERT/Darby | 2021-01-04 |
| 04719873121373 - 30K FS-SLIM PLASTIC INSERT/Darby | 2021-01-04 |
| 04719873121380 - 25K FS-10 PLASTIC INSERT/Darby | 2021-01-04 |
| 04719873121397 - 30K FS-10 PLASTIC INSERT/Darby | 2021-01-04 |
| 04719873121359 - BONE TIP/BM-PS1 | 2020-09-25 |