This page includes the latest FDA filings for Hako Med G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3007967212 |
| FEI Number | 3007967212 |
| Name | N/A |
| Owner & Operator | Hako-Med Gmbh |
| Contact Address | Staigstrasse 1 karlsruhe DE-BW Baden-Wurttemberg 76229 DE |
| Official Correspondent |
|
| US Agent | |
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | N/A N/A N/A, NA N/A US |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
N/A [Hako-Med Gmbh] | PROElecDT series | 2010-12-21 |
N/A [Hako-Med Gmbh] | PROElecDT series | 2010-12-21 |
N/A [Hako-Med Gmbh] | ElecDT/VasoPulse series | 2010-12-21 |
N/A [Hako-Med Gmbh] | ElecDT/VasoPulse series | 2010-12-21 |