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"Koma" Effie two-dose artificial vitreous - Taiwan Registration 169ad7b7038202e418f67e29be95a734

Access comprehensive regulatory information for "Koma" Effie two-dose 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 169ad7b7038202e418f67e29be95a734 and manufactured by VALEANT MED Sp. z o.o.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE 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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169ad7b7038202e418f67e29be95a734
Registration Details
Taiwan FDA Registration: 169ad7b7038202e418f67e29be95a734
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Device Details

"Koma" Effie two-dose artificial vitreous
TW: โ€œๅฏ‡็‘ชโ€่‰พ้ฃ›้›™ๅŠ‘ไบบๅทฅ็Žป็’ƒ้ซ”
Risk Class 3
Cancelled

Registration Details

169ad7b7038202e418f67e29be95a734

DHA00602227304

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

Apr 18, 2011

Apr 18, 2021

Sep 08, 2023

Cancellation Information

Logged out

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