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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
COVIDIEN LP LLC NORTH HAVEN TRI-STAPLE 2.0 11/23/2022
US SURGICAL PUERTO RICO ENDO GIA ULTRA 10/25/2022
COVIDIEN LP LLC NORTH HAVEN ENDO GIA 10/25/2022
US SURGICAL PUERTO RICO GIA 10/18/2022
COVIDIEN LP LLC NORTH HAVEN SIGNIA 09/30/2022
COVIDIEN LP LLC NORTH HAVEN TRI-STAPLE 2.0 09/30/2022
US SURGICAL PUERTO RICO GIA 09/15/2022
COVIDIEN LP LLC NORTH HAVEN GIA 09/06/2022
US SURGICAL PUERTO RICO ENDO GIA ULTRA 08/23/2022
US SURGICAL PUERTO RICO ENDO GIA 08/23/2022
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