| Primary Device ID | 30817357021838 |
| NIH Device Record Key | ac7d5d35-2d9f-46f7-9e7e-e552521b06ef |
| Commercial Distribution Discontinuation | 2019-07-31 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | CTC |
| Version Model Number | VP501L |
| Company DUNS | 177939027 |
| Company Name | HYGIA HEALTH SERVICES, 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 | true |
| 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 |