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 |