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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
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 12/02/2021
ABBOTT VASCULAR XIENCE ALPINE EVEROLIMUS ELUTING CORONAR 11/30/2021
BIOTRONIK AG, BUELACH, SWITZERLAND ORSIRO MISSION 3.5/35 11/24/2021
BIOTRONIK AG, BUELACH, SWITZERLAND ORSIRO MISSION 3.5/18 11/24/2021
BOSTON SCIENTIFIC CORPORATION SYNERGY XD 11/22/2021
ABBOTT VASCULAR XIENCE PROA EVEROLIMUS ELUTING CORONARY 11/16/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 11/08/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 10/28/2021
ABBOTT VASCULAR XIENCE SKYPOINT DRUG ELUTING CORONARY ST 10/26/2021
ABBOTT VASCULAR XIENCE ALPINE OTW EVEROLIMUS ELUTING COR 10/11/2021
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