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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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124 records meeting your search criteria returned- Product Code: MIH Product Problem: No Apparent Adverse Event Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE® TAG® THORACIC ENDOPROSTHESIS 09/25/2017
W.L. GORE & ASSOCIATES GORE® EXCLUDER® AAA ENDOPROSTHESIS 09/15/2017
W.L. GORE & ASSOCIATES GORE® EXCLUDER® AAA ENDOPROSTHESIS 09/13/2017
W.L. GORE & ASSOCIATES GORE® EXCLUDER® AAA ENDOPROSTHESIS 09/05/2017
W.L. GORE & ASSOCIATES GORE® TAG® THORACIC ENDOPROSTHESIS 08/30/2017
ENDOLOGIX INC. AFX 05/17/2017
TRIVASCULAR, INC. OVATION PRIME ABDOMINAL STENT GRAFT SYST 08/31/2016
LOMBARD MEDICAL LTD. AORFIX AAA FLEXIBLE STENT GRAFT 10/29/2015
LOMBARD MEDICAL LTD. AORFIX AAA FLEXIBLE STENT GRAFT 10/14/2015
LOMBARD MEDIAL LTD AORTIX AAA FLEXIBLE STENT GRAFT SYSTEM 06/09/2015
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