Primary Device ID | 07613389658934 |
NIH Device Record Key | 0e435c71-1c5c-4d4b-a954-bae61aecd506 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vista V-UP Select |
Version Model Number | pewter |
Catalog Number | 050-6858-P744 |
Company DUNS | 480662550 |
Company Name | Sonova AG |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |