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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
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45 records meeting your search criteria returned- Product Code: GEI Product Problem: Failure to Conduct Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM 07/03/2018
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM 08/31/2016
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM 08/31/2016
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM 03/02/2016
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL. 03/02/2016
SORIN GROUP USA VASCUCLEAR PRECISION BIPOLAR 11/18/2015
AESCULAP AG CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM 09/29/2015
AESCULAP, INC. CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 07/30/2015
AESCULAP, INC. CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM 07/22/2015
AESCULAP, INC. CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM 04/15/2015
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