| Primary Device ID | D89260705405502 |
| NIH Device Record Key | e720cfef-f468-43fb-a9ab-75d8c6e1bcbb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PROPHY PASTE |
| Version Model Number | 6070540550 |
| Company DUNS | 079343581 |
| Company Name | MAXILL, INC. |
| Device Count | 200 |
| 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 | false |
| 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 |
|---|---|
| HIBCC | D89260705405500 [Unit of Use] |
| HIBCC | D89260705405501 [Primary] |
| HIBCC | D89260705405502 [Package] Contains: D89260705405501 Package: Case [4000 Units] In Commercial Distribution |
| EJR | Agent, Polishing, Abrasive, Oral Cavity |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-28 |
| Device Publish Date | 2022-10-20 |
| D89260705405852 | 6070540585 |
| D89260705405812 | 6070540581 |
| D89260705405762 | 6070540576 |
| D89260705405752 | 6070540575 |
| D89260705405722 | 6070540572 |
| D89260705405712 | 6070540571 |
| D89260705405662 | 6070540566 |
| D89260705405652 | 6070540565 |
| D89260705405622 | 6070540562 |
| D89260705405612 | 6070540561 |
| D89260705405602 | 6070540560 |
| D89260705405502 | 6070540550 |