2,170 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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GOOD NIGHT
FDA 510(k)
FDA Class 2
·Dental
FIDIS CONNECTIVE 8
FDA 510(k)
FDA Class 2
·Immunology
FIDIS TM THYRO, MODEL MX002
FDA 510(k)
FDA Class 2
·Immunology
FIDIS VASCULITIS, MODEL MX007
FDA 510(k)
FDA Class 2
·Immunology
FIDIS CELIAC
FDA 510(k)
FDA Class 2
·Immunology
FIDIS DSDNA
FDA 510(k)
FDA Class 2
·Immunology
FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARIS
FDA 510(k)
FDA Class 2
·Immunology
MODIFICATION TO FIDIS CONNECTIVE 10*, MODEL MX006
FDA 510(k)
FDA Class 2
·Immunology
FIDIS CONNECTIVE 10, MODEL MX006
FDA 510(k)
FDA Class 2
·Immunology
FIDIS VASCULITIS ASSAY KIT AND ANALYZER AND CARIS SYSTEM
FDA 510(k)
FDA Class 2
·Immunology
MODIFICATION TO FIDIS VASCULITIS, MODEL MX007
FDA 510(k)
FDA Class 2
·Immunology
USDL MODEL SELECT 1000 FREQUENCY DOUBLED ND:YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
FLASH AR PENTA / FLASH AR PENTA QUICK
FDA 510(k)
FDA Class 2
·Dental
Endoscopic Fluorescence Camera System (DPM-ENDOCAM-03PF)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
3D Endoscopic Fluorescence Camera System (DPM-ENDOCAM-06PF)
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
I.V. ADMINISTRATION SET CONNECTING DEVICE
FDA 510(k)
FDA Class 2
·General Hospital