RETI-port/scan 21 alpha plus: 1 catalogue number listed by Roland Consult Stasche & Finger GmbH, under Stimulator, Photic, Evoked Response. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Shaanxi. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for RETI-port/scan 21 alpha plus | Listed by | Roland Consult Stasche & Finger GmbH |
| FDA product code | GWE |
| Device type | Stimulator, Photic, Evoked Response |
| Device class | Class 2 |
| Regulation | 21 CFR 882.1890 |
| 510(k) | K023525 |
| Record published | 2023-02-26 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Label carries | manufacturing date, serial number |
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.