| Primary Device ID | 30818087012936 |
| NIH Device Record Key | 18d0af96-8a3e-455d-aec1-ee00c47d2d19 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Propper Steri-Dot Indicators |
| Version Model Number | 36100100 |
| Catalog Number | 36100100 |
| Company DUNS | 001483130 |
| Company Name | PROPPER MANUFACTURING COMPANY, INC. |
| Device Count | 1000 |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |