| Primary Device ID | 00896128002107 |
| NIH Device Record Key | 7746947b-3ca2-4551-8422-f87b66851d0c |
| Commercial Distribution Discontinuation | 2019-11-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | buddy, Power Module |
| Version Model Number | 403-00231A |
| Company DUNS | 078330362 |
| Company Name | BELMONT INSTRUMENT CORPORATION |
| 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 | true |
| OTC Over-The-Counter | false |