| Primary Device ID | B510PM2000M1 |
| NIH Device Record Key | e1171fdc-5d0a-4894-baf9-a92b63060c88 |
| Commercial Distribution Discontinuation | 2028-04-15 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ADVANCED PATIENT MONITOR |
| Version Model Number | PM-2000M |
| Company DUNS | 608736880 |
| Company Name | ADVANCED INSTRUMENTATIONS, INC. |
| 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 | 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 |