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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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223 records meeting your search criteria returned- Product Code: DRF Product Problem: Entrapment of Device Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 03/24/2022
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 03/21/2022
BIOSENSE WEBSTER INC LASSO® NAV ECO VARIABLE CATHETER 02/28/2022
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 02/18/2022
BIOSENSE WEBSTER INC LASSO® NAV ECO VARIABLE CATHETER 02/15/2022
ST. JUDE MEDICAL INQUIRY AFOCUSII¿ (4 F DOUBLE LOOP) CATH 01/27/2022
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 01/10/2022
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 12/29/2021
ST. JUDE MEDICAL ADVISOR¿ HD GRID MAPPING CATHETER, SENSO 12/17/2021
BIOSENSE WEBSTER INC LASSO® NAV ECO CATHETER 12/16/2021
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