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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
 

 
 
3 records meeting your search criteria returned- Product Code: PMP Product Problem: Energy Output Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL DRG IMPLANT 07/19/2023
ABBOTT MEDICAL PROCLAIM(TM) DRG NEUROSTIMULATOR SYSTEM 11/01/2022
ABBOTT MEDICAL PROCLAIM IMPLANTABLE GENERATOR, BATTERY 03/11/2020
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