2 catalogue numbers from MPP-MT, listed by Medical Measurement Systems B.V., Netherlands, under System, Gastrointestinal Motility (Electrical). 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Shanghai. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for MPP-Plus | Listed by | Medical Measurement Systems B.V., Netherlands |
| FDA product code | FFX |
| Device type | System, Gastrointestinal Motility (Electrical) |
| Device class | Class 2 |
| Regulation | 21 CFR 876.1725 |
| Establishment | Exporter |
| Premarket notification | Exempt |
| Record published | 2025-02-21 |
| Record revised | 2018-03-29 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Prescription | Prescription only |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date, manufacturing date, serial number |
| Storage | Handling environment temperature 15 to 30 °C; Handling environment humidity 30 to 70 °C |
| Packaging | Pack of 100, pack of 400 |
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.