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"Willunme" Bayerkeni artificial vitreous - Taiwan Registration 41d84f7e934f0f43e99f6aa02334d41e

Access comprehensive regulatory information for "Willunme" Bayerkeni artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 41d84f7e934f0f43e99f6aa02334d41e and manufactured by VALEANT MED Sp. z o.o.. 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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41d84f7e934f0f43e99f6aa02334d41e
Registration Details
Taiwan FDA Registration: 41d84f7e934f0f43e99f6aa02334d41e
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Device Details

"Willunme" Bayerkeni artificial vitreous
TW: โ€œๅจๅ€ซ็พŽโ€ ๆ‹œ่€ณๅ…‹ๅฐผไบบๅทฅ็Žป็’ƒ้ซ”
Risk Class 3
Cancelled

Registration Details

41d84f7e934f0f43e99f6aa02334d41e

DHA00602322906

Company Information

Poland

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.4275 ็œผๅ…งๅ……ๅกซ็”จๆถฒ้ซ”

import

Dates and Status

Jan 16, 2012

Jan 16, 2022

Jan 03, 2023

Cancellation Information

Logged out

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