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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
 

 
 
5 records meeting your search criteria returned- Product Code: LDD Product Problem: No Device Output Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
SCHILLER AG TEMPUS LS 02/20/2024
SCHILLER AG TEMPUS LS-MANUAL 11/23/2023
SCHILLER AG TEMPUS LS-MANUAL 05/18/2023
SCHILLER AG TEMPUS LS - MANUAL 12/03/2021
PHILIPS MEDICAL SYSTEMS 3 LEAD IEC ECG PATIENT CABLE 12/15/2016
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