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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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12 records meeting your search criteria returned- Product Code: NTE Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
COVIDIEN SPIDER FX 08/24/2021
COVIDIEN SPIDER FX 03/15/2021
COVIDIEN SPIDER FX 11/13/2020
COVIDIEN SPIDER FX 10/30/2020
INVATEC SPA MO.MA 07/09/2020
MEDTRONIC VASCULAR FILTER: SPIDER X EV3 MEDTRONIC 5 06/19/2020
INVATEC SPA MO.MA ULTRA 09/27/2019
COVIDIEN SPIDER FX 09/12/2019
INVATEC SPA MO.MA ULTRA 07/13/2018
COVIDIEN SPIDER FX 07/13/2018
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