This page includes the latest FDA filings for Janelle Herr. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Registration Number | 3001065024 | ||||||||||
FEI Number | 3001065024 | ||||||||||
Name | Janelle Herr | ||||||||||
Owner & Operator | RENFERT GMBH | ||||||||||
Contact Address | UNTERE GIESSWIESEN 2 -- HILZINGEN DE-NOTA 78247 DE | ||||||||||
Official Correspondent |
| ||||||||||
US Agent |
| ||||||||||
Importing Logistics Registration |
| ||||||||||
Registration Status | 1 | ||||||||||
Initial Importer | N | ||||||||||
Registration Expiration | 2020-04-25 | ||||||||||
Registration Address | 3718 Illinois Avenue Saint Charles, IL 60174 US | ||||||||||
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
Janelle Herr [RENFERT GMBH] | temp:ex | 2017-11-13 |
Janelle Herr [RENFERT GMBH] | SYMPRESS | 2007-07-16 |
Janelle Herr [RENFERT GMBH] | SYMPRESS II | 2007-07-16 |
Janelle Herr [RENFERT GMBH] | PROMIX one | 2007-07-16 |
Janelle Herr [RENFERT GMBH] | DUOMIX | 2007-07-16 |
Janelle Herr [RENFERT GMBH] | DUOMIX II | 2007-07-16 |