| Primary Device ID | 10840935109181 |
| NIH Device Record Key | 9ad4512c-0e3d-4d08-ada4-608e56ea7488 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | All Purpose Cuff |
| Version Model Number | 98-0118-03 |
| Company DUNS | 148191133 |
| Company Name | SUNTECH MEDICAL, 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 | true |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |