This page includes the latest FDA filings for Prodimed. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 9615706 |
| FEI Number | 3003781614 |
| Name | PRODIMED PLASTIMED division |
| Owner & Operator | PRODIMED |
| Contact Address | 3 RUE LOUIS ARMAND -- LE PLESSIS BOUCHARD FR-95 Val-dOise 95130 FR |
| Official Correspondent |
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| US Agent |
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| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 6 RUE LOUIS ARMAND LE PLESSIS BOUCHARD Val-dOise, 95130 FR |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
PRODIMED PLASTIMED division [PRODIMED] | COMBICATH CATHETER | 2008-03-20 |
PRODIMED | PRODIMED MICROINJECTION PIPETTES | 1999-06-08 |