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 |
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| US Agent |
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| Importing Logistics Registration |
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| 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 |