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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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11 records meeting your search criteria returned- Product Code: DXE Product Problem: Mechanical Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT DISTA 09/28/2021
INARI MEDICAL INC INARI CLOTTRIEVER SHEATH 06/07/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT PROXI 04/22/2021
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 03/24/2021
ARROW INTERNATIONAL INC. ARROW SEMI-FINISHED KIT: 7FR PTD OTW CAT 10/09/2020
ARROW INTERNATIONAL INC. ARROW SEMI-FINISHED KIT: 7FR PTD OTW CAT 10/09/2020
ARROW INTERNATIONAL INC. ARROW SEMI-FINISHED KIT: 7FR PTD OTW CAT 10/09/2020
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT OMNI 05/08/2020
ARROW INTERNATIONAL INC. ARROW PERCUTANEOUS THROMBOLYTIC DEVICE K 04/27/2020
BOSTON SCIENTIFIC CORPORATION ANGIOJET SOLENT DISTA 03/09/2020
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