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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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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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131 records meeting your search criteria returned- Product Code: NIP Product Problem: Malposition of Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT XL VASCULAR STENT 06/23/2023
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT 5F VASCULAR STENT 06/19/2023
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT 5F VASCULAR STENT 06/19/2023
COVIDIEN EVERFLEX SELF-EXPANDING PERIPHERAL STENT 05/05/2023
COVIDIEN EVERFLEX 04/14/2023
ABBOTT VASCULAR SUPERA SELF-EXPANDING STENT SYSTEM 02/02/2023
BIOTRONIK AG, BUELACH, SWITZERLAND PULSAR-18 T3 6/30/90 11/30/2022
ANGIOMED GMBH & CO. MEDIZINTECHNIK KG LIFESTENT SOLO VASCULAR STENT 11/19/2022
ABBOTT VASCULAR SUPERA 11/18/2022
ABBOTT VASCULAR SUPERA 11/18/2022
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