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"Fasio" IOL guide (unsterilized) - Taiwan Registration 333a1094182fb50b0b4ecf3ef045f164

Access comprehensive regulatory information for "Fasio" IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 333a1094182fb50b0b4ecf3ef045f164 and manufactured by PhysIOL s.a.. The authorized representative in Taiwan is CHIU HO MEDICAL SYSTEM CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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333a1094182fb50b0b4ecf3ef045f164
Registration Details
Taiwan FDA Registration: 333a1094182fb50b0b4ecf3ef045f164
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Device Details

"Fasio" IOL guide (unsterilized)
TW: "ๆณ•่ฅฟๆญ" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

333a1094182fb50b0b4ecf3ef045f164

DHA09401705105

Company Information

Belgium

Product Details

Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

import

Dates and Status

Oct 04, 2016

Oct 04, 2021

Jan 11, 2023

Cancellation Information

Logged out

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