Neurologica Corporation

9 devices* 14 registrations
✕ UK (MHRA) ✕ EU (EUDAMED) ✕ Canada (Health Canada)
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Devices

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Device Name US UK CA AU EU
BodyTom 64 Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
BODYTOM NL 4000 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)
CERETOM, MODEL NL3000 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)
Ceretom Railing System Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
INSPIRA HD, MODEL: NL1000 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)
NExCT 7 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)
OmniTom Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Registered with AU (TGA) Not registered with EU (EUDAMED)
OmniTom Elite 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)
OmniTom Elite with PCD 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)
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