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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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108 records meeting your search criteria returned- Product Code: FDA Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
FUJIFILM CORPORATION EI-530B OR EI-580BT 09/09/2021
FUJIFILM CORPORATION EI-530B 09/09/2021
FUJIFILM CORPORATION EN-450T5/W 09/09/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II SMALL INTESTINAL VIDEOSCOP 08/26/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS LUCERA ELITE SMALL INTESTINALVIDEOS 06/02/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS LUCERA ELITE SMALL INTESTINALVIDEOS 05/31/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II SMALL INTESTINAL VIDEOSCOP 04/14/2021
FUJIFILM CORPORATION FUJIFILM DOUBLE BALLOON ENDOSCOPE EN-580 01/14/2021
FUJIFILM CORPORATION FUJIFILM DOUBLE BALLOON ENDOSCOPE EN-580 01/14/2021
OLYMPUS MEDICAL SYSTEMS CORP. EVIS EXERA II SMALL INTESTINAL VIDEOSCOP 12/03/2020
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