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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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8 records meeting your search criteria returned- Product Code: NIO Product Problem: Patient Device Interaction Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 03/18/2020
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 03/09/2020
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 03/09/2020
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 03/06/2020
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 03/06/2020
W.L. GORE & ASSOCIATES GORE VIABAHN VBX BALLOON EXPANDABLE ENDO 02/29/2020
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG E-LUMINEXX VASCULAR STENT 12/12/2018
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG E-LUMINEXX VASCULAR STENT 10/09/2018
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