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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
 

 
 
6 records meeting your search criteria returned- Product Code: LNH Product Problem: Device-Device Incompatibility Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
GE MEDICAL SYSTEMS, LLC GE 1.5T SIGNA HDX MR SYSTEM 11/02/2021
GE MEDICAL SYSTEMS, LLC SIGNA PIONEER 01/27/2021
GE MEDICAL SYSTEMS, LLC GE 3.0T SIGNA HDX MR SYSTEM 11/12/2020
SIEMENS AG / SIEMENS MEDICAL SOLUTIONS U SIEMENS MRI 08/07/2019
SIEMENS AG / SIEMENS HEALTHCARE GMBH / S MRI 08/05/2019
GE MEDICAL SYSTEMS, LLC 3.0T SIGNA HDX MR SYSTEM 06/20/2019
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