| Primary Device ID | 00858298006583 |
| NIH Device Record Key | eb66bd5f-6bfe-4741-9e78-107a4e54a5e6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Double Pump Kit, Willow Go |
| Version Model Number | PDL60 |
| Company DUNS | 050917861 |
| Company Name | EXPLORAMED NC7, 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 | true |