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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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11 records meeting your search criteria returned- Product Code: DRF Product Problem: Manufacturing, Packaging or Shipping Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
BIOSENSE WEBSTER INC NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER 01/12/2024
BIOSENSE WEBSTER INC NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER 12/28/2023
BIOSENSE WEBSTER INC CELSIUS¿ ELECTROPHYSIOLOGY CATHETER 11/08/2023
BIOSENSE WEBSTER INC LASSOSTAR NAV CIRCULAR MAPPING CATHETER 10/19/2023
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 10/09/2023
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 09/12/2023
BIOSENSE WEBSTER INC NAVISTAR¿ ELECTROPHYSIOLOGY CATHETER 07/20/2023
BIOSENSE WEBSTER INC DECANAV ELECTROPHYSIOLOGY CATHETER 04/12/2023
IRVINE BIOMEDICAL, INC. A ST. JUDE MEDIC INQUIRY STEERABLE DIAGNOSTIC CATHETER 08/20/2021
MPRI STABLEMAPR 06/29/2018
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