| Primary Device ID | 00062790820039 |
| NIH Device Record Key | 3480a7d6-5b80-40a9-8e83-060d4b6763d0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Integrity Amplitrode |
| Version Model Number | A82 |
| Company DUNS | 201740425 |
| Company Name | Vivosonic Inc |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00062790820039 [Primary] |
| EWO | Audiometer |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
| 00062790820039 | Dual channel Amplitrode for use as an accessory with the second generation Integrity V500 system |
| 00062790820022 | One channel Amplitrode for use as an accessory with the second generation of the Integrity V500 |
| 00062790810023 | One channel Amplitrode for use as an accessory with the first generation Integrity V500 system ( |
| 00627908020031 | Dual channel Amplitrode for use as an accessory with the second generation Integrity V500 system |
| 00627908020024 | One channel Amplitrode for use as an accessory with the second generation of the Integrity V500 |
| 00627908010025 | One channel Amplitrode for use as an accessory with the first generation Integrity V500 system ( |