| Primary Device ID | 00860011763208 |
| NIH Device Record Key | 7c70f1fe-7fa2-46f3-afc3-5e9402b4cc68 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NDDR and CDCS |
| Version Model Number | 2.3 |
| Company DUNS | 102958199 |
| Company Name | CIELOWORKS, 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 | true |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| 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 |