Primary Device ID | 03770033463031 |
NIH Device Record Key | a15f73dd-eaa4-46ed-aaf4-21b975ca18af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FETOLY |
Version Model Number | 2 |
Company DUNS | 274279654 |
Company Name | DIAGNOLY |
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 | 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 | true |
OTC Over-The-Counter | false |