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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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64 records meeting your search criteria returned- Product Code: GAW Product Problem: Material Twisted/Bent Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
DAVIS & GECK CARIBE LTD SURGIPRO II 01/21/2020
B.BRAUN SURGICAL SA OPTILENE 6/0 (0,7) 75CM 2XDR10 CV RCP 01/02/2020
B.BRAUN SURGICAL SA OPTILENE 6/0 (0,7) 75CM 2XDR10 CV RCP 01/02/2020
DAVIS & GECK CARIBE LTD UNKNOWN SURGIPRO 12/02/2019
DAVIS & GECK CARIBE LTD SURGIPRO LL 08/22/2019
B.BRAUN SURGICAL SA OPTILENE 7/0 (0,5) 60CM 2XDR10 CV RCP 08/08/2019
DAVIS & GECK CARIBE LTD SURGIPRO LL 03/14/2019
DAVIS & GECK CARIBE LTD SURGIPRO LL 12/12/2018
DAVIS & GECK CARIBE LTD SURGIPRO LL 12/12/2018
B. BRAUN SURGICAL SA OPTILENE 5/0 (1) 90CM 2XHR22 CV RCP 09/14/2018
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