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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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500 records meeting your search criteria returned. The results are incomplete - please narrow your search.

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ManufacturerBrand NameDate Report Received
COCHLEAR LTD NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM 04/21/2022
COCHLEAR LIMITED NUCLEUS CI512 COCHLEAR IMPLANT WITH CONT 04/13/2022
COCHLEAR LTD NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADV 04/11/2022
COCHLEAR LTD NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADV 04/11/2022
COCHLEAR LIMITED NUCLEUS CI632 PROFILE PLUS WITH SLIM MOD 03/24/2022
COCHLEAR LIMITED NUCLEUS CI632 PROFILE PLUS WITH SLIM MOD 03/24/2022
COCHLEAR LIMITED NUCLEUS CI422 COCHLEAR IMPLANT WITH SLIM 03/21/2022
COCHLEAR LTD NUCLEUS CI522 COCHLEAR IMPLANT WITH SLIM 03/17/2022
COCHLEAR LIMITED NUCLEUS CI512 COCHLEAR IMPLANT WITH CONT 03/15/2022
COCHLEAR LTD NUCLEUS CI532 COCHLEAR IMPLANT WITH SLIM 03/14/2022
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