10,000 results
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DRG:HYBRiD.XL®
FDA UDI
DRG Instruments Gesellschaft mit beschränkter Haftung·00404847452525·The DRG:HYBRiD-XL® is a fully automated random ...
DRG:HYBRiD.XL®
FDA UDI
DRG International Inc·00840239052520·The DRG:HYBRiD-XL® is a fully automated random ...
DRG:HYBRiD.XL®
FDA UDI
DRG Instruments Gesellschaft mit beschränkter Haftung·04048474052527·The DRG:HYBRiD-XL® is a fully automated random ...
Tracer Hybrid
FDA UDI
COOK INCORPORATED·00827002226593·Tracer Hybrid Wire Guide
Tracer Hybrid
FDA UDI
COOK INCORPORATED·00827002226616·Tracer Hybrid Wire Guide
ACCESS HYBRITECH PSA
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code LTJ·April 15, 2012
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code LTJ·August 30, 2011
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002237701·Zenapro Hybrid Hernia Repair Device
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002354774·Zenapro Hybrid Hernia Repair Device
Tracer Hybrid
FDA UDI
COOK INCORPORATED·00827002226623·Tracer Hybrid Wire Guide
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002354767·Zenapro Hybrid Hernia Repair Device
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002237718·Zenapro Hybrid Hernia Repair Device
Tracer Hybrid
FDA UDI
COOK INCORPORATED·00827002226609·Tracer Hybrid Wire Guide
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002354798·Zenapro Hybrid Hernia Repair Device
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002237725·Zenapro Hybrid Hernia Repair Device
Zenapro
FDA UDI
COOK BIOTECH INCORPORATED·10827002351148·Zenapro Hybrid Hernia Repair Device
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code LTJ·April 3, 2012
UNICEL DXL800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·April 3, 2012
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LTJ·April 22, 2011
UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LTJ·December 21, 2009