| Primary Device ID | 07613389793895 |
| NIH Device Record Key | cf0e6a36-09af-433f-a842-769ad70a6bf3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GEERS 4 |
| Version Model Number | 4.0 |
| Catalog Number | 088-0027-00040 |
| 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 |