This page includes the latest FDA filings for Zurich Medical Headquarters. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3013943846 |
| FEI Number | 3013943846 |
| Name | Zurich Medical Headquarters |
| Owner & Operator | Zurich Medical |
| Contact Address | 2445 Xenium Ln N Plymouth MN 55441 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2445 Xenium Ln N Plymouth, MN 55441 US |
| Establishment Type | Manufacture Device in the United States for Export Only |
Device Company | Device | Date |
|---|---|---|
Zurich Medical Headquarters [Zurich Medical] | Zurich Pressure Guidewire System Model 100 | 2020-02-27 |
Zurich Medical Headquarters [Zurich Medical] | Zurich Pressure Guidewire System Model 100 | 2020-02-27 |
Zurich Medical Headquarters [Zurich Medical] | Zurich Pressure Guidewire System Model 100 | 2020-02-27 |
Zurich Medical Headquarters [Zurich Medical] | Zurich Pressure Guidewire System Model 100 | 2020-02-27 |
Zurich Medical Headquarters [Zurich Medical] | Zurich Pressure Guidewire System Model 100 | 2019-06-13 |