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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
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10 records meeting your search criteria returned- Product Code: KPR Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. MULTIDIAGNOST ELEVA 07/02/2021
SIEMENS HEALTHCARE GMBH YSIO MAX 04/26/2021
SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD MULTIX FUSION 03/26/2021
SIEMENS HEALTHCARE GMBH YSIO 02/24/2021
SIEMENS HEALTHCARE GMBH AXIOM ARISTOS FX PLUS 09/18/2020
SEDECAL SA GE 09/11/2020
GE HANGWEI MEDICAL SYSTEMS CO., LTD. PROTEUS XR/A RADIOGRAPHIC SYSTEM 10/28/2019
GE HANGWEI MEDICAL SYSTEMS CO., LTD. PROTEUS XR/A RADIOGRAPHIC SYSTEM 07/29/2019
SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD MULTIX SELECT DR 04/25/2019
PHILIPS HEALTHCARE MULTIDIAGNOST ELEVA 09/21/2016
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