This page includes the latest FDA filings for Gore European Warehouse Support. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3015138222 |
| FEI Number | 3015138222 |
| Name | Gore European Warehouse Support |
| Owner & Operator | W. L. GORE & ASSOCIATES, INC. |
| Contact Address | 3250 W. Kiltie Lane Flagstaff AZ 86005 US |
| 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 | Doctor Paul Janssenweg 150 Tilburg Noord-Brabant, 5026 NL |
| Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
|---|---|---|
Gore European Warehouse Support [W. L. GORE & ASSOCIATES, INC.] | GORE? Molding and Occlusion Balloon Catheter | 2018-02-08 |
Gore European Warehouse Support [W. L. GORE & ASSOCIATES, INC.] | GORE DRYSEAL FLEX INTRODUCER SHEATH | 2016-05-13 |