Primary Device ID | 05060630100025 |
NIH Device Record Key | 5f5f2a1e-b82c-463a-8373-3556205c4f64 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Flo |
Version Model Number | NNTAMP01 |
Company DUNS | 222200021 |
Company Name | HERE WE FLO LTD |
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 | false |
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 |