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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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9 records meeting your search criteria returned- Product Code: LDD Product Problem: Mechanical Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SCHILLER AG TEMPUS LS-MANUAL 12/01/2023
SCHILLER AG TEMPUS LS-MANUAL 11/24/2023
SCHILLER AG TEMPUS LS-MANUAL 11/22/2023
SCHILLER AG TEMPUS LS-MANUAL 10/31/2023
SCHILLER AG TEMPUS LS MANUAL 10/20/2023
SCHILLER AG TEMPUS LS-MANUAL 09/13/2023
SCHILLER AG TEMPUS LS-MANUAL 07/12/2023
PHILIPS MEDICAL SYSTEMS SMALL SWITCHED INT PDLS 07/08/2014
PHYSIO-CONTROL, INC LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR 01/13/2014
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