The Battery system is a device which allows supply an energy to prosthetic hand . The Aether Battery System consists of a battery pack AET-BAT with the necessary interconnections.
Who Else Makes It
Concentrated in Guangdong (3), Shanghai (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Aether Battery System | Listed by | Aether Biomedical SP. Z O.O., Poland |
| FDA product code | IQZ |
| Device type | Hand, External Limb Component, Powered |
| Device class | Class 1 |
| Regulation | 21 CFR 890.3420 |
| Establishment | Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2023-01-31 |
| Record revised | 2023-08-17 (version 4) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Label carries | expiry date, manufacturing date, serial number |
| Storage | Storage environment temperature 0 to 50 °C |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.