Inari Medical, Inc.

6001 Oak Canyon, Suite 100, Irvine, United States, 92618

75 devices* 121 registrations
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Devices

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Showing 1–20 of 75 devices

Device Name US UK CA AU EU
518259 MDR2017P Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Artix AX Registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
Artix AX, 115 cm Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Artix AX, 85 cm Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Artix Ballon Guiding Sheath Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Artix BG Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
ARTIX MT Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Artix MT6 Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Artix MT8 Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
Artix™ MT; Artix™ Thin-Walled Thrombectomy Sheath Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
Artix MT, MT6 Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Artix MT, MT8 Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
ARTIX THIN-WALLED SHEATH Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
Artix Thin-Walled Sheath (65 cm) Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Artix Thin-Walled Sheath, 90 cm Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
Artix Thrombectomy Device Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
ClotTriever Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
ClotTriever BOLD Catheter Registered with US (FDA) Registered with UK (MHRA) Registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
ClotTriever Catheter Not registered with US (FDA) Registered with UK (MHRA) Registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
ClotTriever Sheath Registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Registered with EU (EUDAMED)
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