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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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20 records meeting your search criteria returned- Product Code: DWS Product Problem: Mechanical Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ATRICURE, INC. UNIVERSAL STABILIZER ARM, HERCULES 3 05/01/2018
MAQUET CV ULTIMA ACTIVATOR II REUSABLE DRIVE MECH. 05/12/2017
MAQUET CV ULTIMA OPCAB SYSTEM, STANDARD BLADE 08/15/2016
MAQUET CV ULTIMA OPCAB SYSTEM, STANDARD BLADE 09/18/2015
MAQUET CARDIOVASCULAR LLC ULTIMA ACTIVATOR II REUSABLE DRIVE MECH 08/06/2015
MAQUET CARDIOVASCULAR, LLC MIRA-I CS RETRACTOR BODY 04/13/2015
MAQUET CARDIOVASCULAR, LLC ULTIMA ACTIVATOR II REUSABLE DRIVE MECH 10/09/2014
MAQUET CARDIOVASCULAR, LLC ULTIMA ACTIVATOR II REUSABLE DRIVE MECH. 05/02/2014
TELEFLEX PILLING AORTIC PUNCH STD TIP 5.0 04/28/2014
TELEFLEX PILLING AORTIC PUNCH STD TIP 5.0 04/28/2014
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