Primary Device ID | EFIAE0135162 |
NIH Device Record Key | 3c9bb77b-9e69-4e48-8c8f-fdd5e18dbbd0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VenSure Nav Balloon Sinus Dilation System |
Version Model Number | 1 |
Company DUNS | 312623008 |
Company Name | Fiagon GmbH |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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