This page includes the latest FDA filings for Medizintechnik Gulden. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3001281099 | ||||||
| FEI Number | 3001281099 | ||||||
| Name | MEDIZINTECHNIK GULDEN | ||||||
| Owner & Operator | MEDIZINTECHNIK GULDEN | ||||||
| Contact Address | ESCHENWEG 3 -- MODAUTAL DE-HE Hessen 64397 DE | ||||||
| US Agent |
| ||||||
| Importing Logistics Registration |
| ||||||
| Registration Status | 1 | ||||||
| Initial Importer | N | ||||||
| Registration Expiration | 2020-04-25 | ||||||
| Registration Address | ESCHENWEG 3 MODAUTAL Hessen, 64397 DE | ||||||
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
MEDIZINTECHNIK GULDEN | Periotest | 2007-11-17 |