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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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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
ABBOTT / ABBOTT VASCULAR ABBOTT SUPERA STENT 02/17/2021
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 02/12/2021
BIOTRONIK AG, BUELACH, SWITZERLAND ASTRON 9/40/120 12/10/2020
COVIDIEN PROTEGE EVERFLEX SELF-EXPANDING STENT SY 11/09/2020
ABBOTT VASCULAR ABSOLUTE PRO VASCULAR SELF-EXPANDING STE 11/04/2020
W. L. GORE & ASSOCIATES, INC. GORE VIABAHN ENDOPROSTHESIS WITH HEPARIN 09/04/2020
W. L. GORE & ASSOCIATES, INC. GORE VIABAHN ENDOPROSTHESIS 08/12/2020
ABBOTT VASCULAR SUPERA 6F 08/06/2020
W.L. GORE & ASSOCIATES, INC. VIABAHN GORE CARDIAC STENT 07/21/2020
COVIDIEN EVERFLEX SELF-EXPANDING PERIPHERAL STENT 12/13/2019
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