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

 
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111 records meeting your search criteria returned- Product Code: GEI Product Problem: Failure to Shut Off Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
MAQUET CARDIOVASCULAR LLC VASO VIEW HEMOPRO 04/02/2019
MEDTRONIC ADVANCED ENERGY, LLC PULSAR FOOTSWITCH-WIRELESS 03/28/2019
MEDTRONIC ADVANCED ENERGY (SALIENT) AEX GENERATOR-REFURB 03/27/2019
MEDTRONIC ADVANCED ENERGY, LLC UNKNOWN PLASMABLADE DEVICE 03/27/2019
MAQUET CARDIOVASCULAR LLC VASO VIEW HEMOPRO 03/25/2019
MEGADYNE MEDICAL PRODUCTS, INC. MEGAPOWER 1000 A GENERATOR 03/05/2019
DEROYAL INDUSTRIES, INC. CAUTERY PENCIL 02/05/2019
MAQUET CV VASO VIEW HEMOPRO 02/01/2019
MEDTRONIC ADVANCED ENERGY (SALIENT) AQUAMANTYS 6.0 BIPOLAR SEALER 01/31/2019
MEDTRONIC ADVANCED ENERGY, LLC AQUAMANTYS GENERATOR (115V) 01/31/2019
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