Ophtec BV

Schweitzerlaan 15, Groningen, Netherlands, 9728 NR

35 devices* 45 registrations
✕ EU (EUDAMED)
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Devices

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Showing 1–20 of 35 devices

Device Name US UK CA AU EU
ARTIFLEX INSERTION SPATULA Not registered with US (FDA) Registered with UK (MHRA) Registered with Canada (Health Canada) AU (TGA): manufacturer registered, device not confirmed Not registered with EU (EUDAMED)
ARTIFLEX Myopia 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)
ARTIFLEX MYOPIA INTRAOCULAR LENS 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)
ARTIFLEX Toric S**.*C-*.*X0Ø 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)
ARTIFLEX Toric S**.*C-*.*X90Ø 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)
Artiplus Toric 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)
ARTISAN Aphakia 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)
ARTISAN Aphakia 5/8.5 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)
ARTISAN ENCLAVATION NEEDLE 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)
ARTISAN HYPEROPIA 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)
ARTISAN Hyperopia 5/8.5 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)
ARTISAN Myopia 5/8.5 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)
ARTISAN Myopia 6/8.5 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)
ARTISAN Myopia Models 204US1W and 206US1W 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)
ARTISAN MYOPIA PHAKIC INTRAOCULAR LENS 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)
ARTISAN Toric Sxx*Cxx*0Ø 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)
ARTISAN Toric Sxx*Cxx*90Ø 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)
CAPSULAR TENSION RING 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)
Capsular Tension Ring 12/10 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)
Capsular Tension Ring 13/11 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)
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