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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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176 records meeting your search criteria returned- Product Code: GEI Product Problem: Loss of or Failure to Bond Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
DEPUY MITEK LLC US VAPR P50 W/ HAND CONTROLS 10/16/2020
COVIDIEN LP LIGASURE 10/01/2020
DEPUY MITEK LLC US VAPR PREMIERE50 ELECTRODE -EA 09/30/2020
DEPUY MITEK LLC US S50 SM.DIA.ELECTRODE W/INTEG.HNDPIECE-EA 09/30/2020
DEPUY MITEK LLC US VAPR CLPLSE90 ELECTRODE W HAND CNTRLS 09/21/2020
DEPUY MITEK LLC US VAPR CLPLSE90 ELECTRODE W HAND CNTRLS 09/21/2020
DEPUY MITEK LLC US VAPR S90 4.0MM W/INTEGR HDP -EA 09/08/2020
DEPUY MITEK LLC US VAPR VUE GENERATOR 09/03/2020
DEPUY MITEK LLC US VAPR VUE GENERATOR 08/07/2020
MAQUET CARDIOVASCULAR LLC VASOVIEW HEMOPRO 2 07/28/2020
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