Primary Device ID | 07613389793956 |
NIH Device Record Key | 0677a727-d4f5-48a0-baa4-cc504106d499 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GEERS 4 |
Version Model Number | 4.2 |
Catalog Number | 088-0027-00042 |
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 | 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 | false |
OTC Over-The-Counter | false |