Catalogue number CY-1000-240, listed by Motive Health, Inc., United States, under Goniometer, Ac-Powered. 4 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Guangdong (2), Zhejiang (1), Shanghai (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for e-vive Nmes System; Large/XL, Right, Bilateral Kit | Listed by | Motive Health, Inc., United States |
| FDA product code | KQX |
| Device type | Goniometer, Ac-Powered |
| Device class | Class 1 |
| Regulation | 21 CFR 888.1500 |
| Establishment | Specification developer, Manufacturer |
| 510(k) | K163067 |
| Record published | 2019-03-31 |
| Record revised | 2023-06-02 (version 7) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Storage | Storage environment temperature -25 to 70 °C; Storage environment humidity 10 to 90 % RH; Storage environment atmospheric pressure 50 to 106 KiloPascal; Handling environment temperature -25 to 70 °C; Handling environment humidity 10 to 90 % RH; Handling environment atmospheric pressure 50 to 106 KiloPascal |
| Sizes | Length 16 in |
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.