ADI 9000/9001 ARTHROSCOPE AND ACCESSORIES

FDA 510(k)

FDA Class 2 ·Orthopedic

Device, Hemostasis, Vascular

FDA Pre-Market Approval

FDA Class 3 ·MYNX CADENCE VASCULAR CLOSURE DEVICE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755353·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350754714·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350754752·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350756114·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755377·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755919·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755711·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350756152·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755896·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755476·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755759·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350756138·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755513·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350756091·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350772695·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350756015·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755230·RADIFOCUS GLIDEWIRE

GLIDEWIRE

FDA UDI

TERUMO CORPORATION·04987350755155·RADIFOCUS GLIDEWIRE