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 |