PMDA registration
Sysmex Europe SE
PMDA registration EG21380191 · Germany
Key facts
| Registration number | EG21380191 |
|---|---|
| Site | Sysmex Europe SE |
| Corporation | Sysmex Europe GmbH |
| Country | Germany |
| Type of business | Foreign manufacturers of in vitro diagnostic drugs |
| Registration categories | In vitro diagnostic drug registration |
| Registered | Oct 22, 2022 |
| Expires | Oct 21, 2027 |
At a glance
- None PMDA inspections
- No Registration expired
- No Registration abolished
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMDA registered foreign manufacturers (Japan)
Foreign manufacturers of drugs and medical devices supplied to Japan must be registered (accredited) with the Ministry of Health, Labour and Welfare through the PMDA.
Source: Pharmaceuticals and Medical Devices Agency (PMDA), Japan