| Primary Device ID | D112POLIDCPW2BF1 |
| NIH Device Record Key | 2959c932-f8b4-42c3-8c44-df4aa25f0f0e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STRAUSS DIAMOND |
| Version Model Number | POLIDCPW2BF |
| Company DUNS | 045784021 |
| Company Name | Diamond Strauss Instruments 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 | false |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | D112POLIDCPW2BF1 [Primary] |
| EJR | Agent, Polishing, Abrasive, Oral Cavity |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
[D112POLIDCPW2BF1]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-24 |
| Device Publish Date | 2022-10-14 |