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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
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82 records meeting your search criteria returned- Product Code: NIP Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 12/15/2015
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 12/15/2015
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 09/18/2015
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 07/28/2015
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 06/11/2015
ABBOTT LABORATORIES SUPERA PERIPHERAL STENT 6.5MM X 88MM 12/09/2014
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT VASCULAR STENT SYSTEM 11/25/2014
W.L. GORE & ASSOCIATES,INC GORE VIABAHN 10/09/2014
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 05/21/2014
W.L. GORE & ASSOCIATES GORE VIABAHN® ENDOPROSTHESIS 05/12/2014
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