6 results
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15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Other
×
CENTRAL VENOUS CATHETER
FDA Adverse Event
Other
·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 2, 1999
CD1700 CS
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·August 3, 1999
1415939-1999-00013
FDA Adverse Event
Other
·December 23, 1999
PHERES-FLOW CENTRAL VENOUS CATHETER KIT
FDA Adverse Event
Other
·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC.·Product code FJS·December 3, 1999
AORTIC OCCLUSION CATHETER
FDA Adverse Event
Other
·HORIZON MEDICAL PRODUCTS, INC.·Product code MJN·October 26, 1999
CIRCLE C SILICONE CATHETER KIT
FDA Adverse Event
Other
·NEOSTAR MEDICAL TECHNOLOGIES/HORIZON MEDICAL PRODUCTS, INC·Product code FJS·October 26, 1999