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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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78 records meeting your search criteria returned- Product Code: LDD Product Problem: Failure to Deliver Shock/Stimulation Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
SCHILLER AG TEMPUS LS 06/22/2023
ZOLL MEDICAL CORPORATION ASSY, ATCLVBL, INT HANDLES, W/BTN, W/16F 06/09/2023
ZOLL MEDICAL CORPORATION ASSY, ATCLVBL, INT HANDLES, W/BTN, W/16F 06/09/2023
REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS LS 06/08/2023
ZOLL MEDICAL CORPORATION AUTOCLAVABLE INTERNAL HANDLES (MSERIES) 06/08/2023
ZOLL MEDICAL CORPORATION AUTOCLAVABLE INTERNAL HANDLES (MSERIES) 06/07/2023
SCHILLER AG TEMPUS 05/10/2023
SCHILLER AG TEMPUS LS-MANUAL 04/25/2023
FIAB SPA EURODEFIPADS 04/19/2023
SCHILLER AG TEMPUS LS MAN DEFIBRILLATOR 04/12/2023
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