| Primary Device ID | D716PULTRAPZHP1 |
| NIH Device Record Key | a2ab4a8f-a113-46ef-8481-3a5bdef4588f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProUltra Piezo |
| Version Model Number | PULTRAPZHP |
| Catalog Number | PULTRAPZHP |
| Company DUNS | 942778564 |
| Company Name | TULSA DENTAL PRODUCTS LLC |
| 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 | false |
| 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 |
|---|---|
| HIBCC | D716PULTRAPZHP1 [Primary] |
| ELC | Scaler, ultrasonic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
[D716PULTRAPZHP1]
Liquid Chemical
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-25 |
| Device Publish Date | 2022-10-17 |
| D716PULTRAPZHP1 | ProUltra Piezo Handpiece |
| D716PULTRAPZ1 | ProUltra Piezo Ultrasonic |