Nerveäna+®: 4 catalogue numbers listed by Neurovision Medical Products, Inc., United States, under Electrode, Needle, Diagnostic Electromyograph. 2 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Shandong (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Nerveäna+® | Listed by | Neurovision Medical Products, Inc., United States |
| FDA product code | IKT |
| Device type | Electrode, Needle, Diagnostic Electromyograph |
| Device class | Class 2 |
| Regulation | 21 CFR 890.1385 |
| Establishment | Manufacturer |
| Record published | 2023-04-11 |
| Record revised | 2025-09-08 (version 3) |
Specifications
Specifications | MRI safety | MR Unsafe |
| Supplied sterile | Yes |
| Single use | Yes |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 5 |
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.