63 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HARVEST TECHNOLOGIES DUAL LIQUID APPLICATOR, MODEL SK/S: HARVEST DUAL LIQUID APPLICATOR LK/2
FDA 510(k)
FDA Class 2
·General Hospital
Affiniti
FDA UDI
TORNIER, INC.·00846832024810·GLENOID REAMER
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741104244·Catheter Placement Kit
Zavation
FDA UDI
Zavation LLC·00842166167605·4-Level, 56mm Cervical Plate
GeneXpert Infinity-80 System
FDA UDI
CEPHEID·07332940006853·Additional catalog number: 900-0456R
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167700004560·
PenEvac1
FDA UDI
I.C. MEDICAL, INC.·00817688020066·
CURE™ ACP
FDA UDI
MEDITECH SPINE, LLC·B167S1700004560·
BIO-LIPID HUMAN SERUM HDL AND LDL CALIBRATORS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
SMART SHIELD NON-STERILE POWDER-FREE PEPPERMINT SCENTED GREEN LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 11, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code NKB·June 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·May 18, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·December 17, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·December 17, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·December 17, 2010
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·May 6, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·August 6, 2010