Primary Device ID | 07613389775860 |
NIH Device Record Key | 83f0ea1c-384e-4eda-9937-cf8f26d4c5fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MEMINI E 4 5P R-R PH |
Version Model Number | (silver gray) |
Catalog Number | 050-1049-P6B1 |
Company DUNS | 480662550 |
Company Name | Sonova AG |
Device Count | 1 |
DM Exempt | false |
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 | false |
OTC Over-The-Counter | false |