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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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82 records meeting your search criteria returned- Product Code: JAK Patient Problem: Insufficient Information Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
PHILIPS ELECTRONICS LTD PHILIPS IQON CT SCANNER 07/15/2022
SIEMENS AG/SIEMENS HEALTHCARE GMBH SYSTEM, X-RAY, TOMOGRAPHY, COMPUTED 07/05/2022
SIEMENS AG/SIEMENS HEALTHCARE GMBH SENSATION 64 06/27/2022
COVIDIEN LP ILLUMISITE 06/17/2022
SIEMENS AG/SIEMENS HEALTHCARE GMBH SENSATION 64 06/16/2022
VERAN MEDICAL TECHNOLOGIES, INC SPIN PLANNING LAPTOP WORKSTATION 06/06/2022
SIEMENS HEALTHCARE GMBH SOMATOM DEFINITION AS 05/10/2022
GE HEALTHCARE JAPAN CORPORATION GE OPTIMA CT660 TRAUMA SCANNER 03/22/2022
SIEMENS MEDICAL SOLUTIONS USA, INC SOMATOM SENSATION 64 03/17/2022
VERAN MEDICAL TECHNOLOGIES, INC SPIN DRIVE SOFTWARE 03/15/2022
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