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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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8 records meeting your search criteria returned- Product Code: MHE Product Problem: No Device Output Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
COCHLEAR LTD NUCLEUS 24 ABI 08/26/2022
COCHLEAR LTD NUCLEUS 24 ABI 04/20/2021
COCHLEAR LTD NUCLEUS 24 ABI 05/15/2019
COCHLEAR LTD. NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SY 10/07/2016
COCHLEAR LTD. NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SY 08/22/2016
COCHLEAR LTD. NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SY 09/10/2015
COCHLEAR LTD . NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SY 07/02/2015
COCHLEAR LTD . NUCLEUS 24 AUDITORY BRAINSTEM IMPLANT SY 07/02/2015
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