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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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72 records meeting your search criteria returned- Product Code: LWP Product Problem: Device Contamination With Biological Material Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
CPI PLANT - ST. PAUL ACUITY 07/10/2017
CPI PLANT - ST. PAUL ACUITY 07/10/2017
CPI PLANT - ST. PAUL ACUITY 07/10/2017
GUIDANT CRM CLONMEL IRELAND INGENIO 04/19/2017
CPI PLANT - ST. PAUL ACUITY 04/12/2017
GUIDANT CRM CLONMEL IRELAND COGNIS 04/11/2017
GUIDANT PUERTO RICO BV AUTOGEN 01/31/2017
GUIDANT CRM CLONMEL IRELAND INGENIO 01/20/2017
GUIDANT CRM CLONMEL IRELAND INCEPTA 01/17/2017
GUIDANT CRM CLONMEL IRELAND ACCOLADE 01/11/2017
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