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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
 

 
 
9 records meeting your search criteria returned- Product Code: IZI Product Problem: Radiation Overexposure Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
Unknown Manufacturer ALLURA XPER FD 05/06/2021
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. ALLURA XPER FD20/10 & ALLURA XPER FD20/2 10/22/2020
PHILIPS HEALTHCARE ALLURA XPER FD10 09/14/2020
PHILIPS HEALTHCARE ALLURA XPER FD10 08/30/2017
PHILIPS HEALTHCARE ALLURA XPER FD10 08/07/2017
PHILIPS HEALTHCARE ALLURA XPER FD10 08/03/2017
GE MEDICAL SYSTEMS SCS INNOVA IGS 530 04/07/2016
GE MEDICAL SYSTEMS SCS INNOVA IGS 540 12/26/2014
PHILIPS HEALTHCARE ALLURA XPER FD20 BIPLANE 05/21/2014
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