Data / Medical devices / Netherlands / Medical Measurement Systems B.V.
Medical Measurement Systems B.V.: FDA-registered device maker in HENGELO Overijssel, Netherlands, 6 510(k) clearances
Medical Measurement Systems B.V. is registered with the FDA (registration 9611896) in HENGELO Overijssel, Netherlands. It lists 6 device types. The FDA files 6 510(k) clearances under its listings, the newest dated August 1, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9611896
- FEI number
- 3002957361
- Address
- Expolaan 50, HENGELO Overijssel, Netherlands, 7556 BE
- Owner or operator
- MEDICAL MEASUREMENT SYSTEMS B.V. (9011630)
- Roles
- Exporter to the US
- First device listed
- November 3, 1999
- Registered through
- 2026
- Brand names listed
- Flowmaster, Flowstar, Ohmega, Solar Blue, Nexam, Solar GI, Solar GI with CIM-AUX, Solar GI with MMP Plus, Solar GI with MMS Video Option, Solar GI with Neuro Module
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cystometer, Electrical Recording | EXQ | 2 | Exporter to the US | accessdata.fda.gov |
| Device, Cystometric, Hydraulic | FEN | 2 | Exporter to the US | accessdata.fda.gov |
| Device, Nerve Conduction Velocity Measurement | JXE | 2 | Exporter to the US | accessdata.fda.gov |
| Stimulator, Electrical, Evoked Response | GWF | 2 | Exporter to the US | accessdata.fda.gov |
| System, Gastrointestinal Motility (Electrical) | FFX | 2 | Exporter to the US | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Exporter to the US | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 1, 2012 | K121014 | SOLAR GI | FFX | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
| April 21, 2006 | K060166 | OHMEGA | FFX | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
| December 15, 2005 | K052338 | SOLAR GI | FFX | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
| May 26, 2005 | K050993 | MMS VIDEO OPTION | LLZ | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
| March 19, 2004 | K031084 | SOLAR GI SYSTEM | FFX | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
| March 3, 2004 | K031930 | HIGH SPEED EMG MODULE | GWF | Substantially Equivalent | Medical Measurement Systems B.V. | accessdata.fda.gov |
Compare with other makers
- All makers of Cystometer, Electrical Recording
- All makers of System, Gastrointestinal Motility (Electrical)
- All makers of Device, Cystometric, Hydraulic
- All makers of Stimulator, Electrical, Evoked Response
- All makers of Device, Nerve Conduction Velocity Measurement
- All makers of System, Image Processing, Radiological
Updated August 1, 2012. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.