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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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81 records meeting your search criteria returned- Product Code: IYN Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON S2000 ULTRASOUND SYSTEM 12/14/2018
SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON S2000 ULTRASOUND SYSTEM 12/14/2018
Unknown Manufacturer ULTRASOUND SCANNER 09/28/2018
SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON SEQUOIA S512 ULTRASOUND SYSTEM 06/08/2018
Unknown Manufacturer ULTRASOUND IMAGING SYSTEM 03/06/2018
FUJIFILM SONOSITE, INC. EDGE ULTRASOUND SYSTEM, 1.2.3, ROHS 12/22/2017
PHILIPS ULTRASOUND, INC. SPARQ 06/06/2017
SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON S2000 ULTRASOUND SYSTEM 04/11/2017
SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON X700 ULTRASOUND SYSTEM 02/08/2017
Unknown Manufacturer ULTRASOUND IMAGING SYSTEM 01/31/2017
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