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"Koma" Mingjia artificial vitreous - Taiwan Registration e2a395c7b2e8bc44c1cda7d6a0bce12f

Access comprehensive regulatory information for "Koma" Mingjia 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 e2a395c7b2e8bc44c1cda7d6a0bce12f 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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e2a395c7b2e8bc44c1cda7d6a0bce12f
Registration Details
Taiwan FDA Registration: e2a395c7b2e8bc44c1cda7d6a0bce12f
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Device Details

"Koma" Mingjia artificial vitreous
TW: โ€œๅฏ‡็‘ชโ€ๆ˜Žไฝณไบบๅทฅ็Žป็’ƒ้ซ”
Risk Class 3
Cancelled

Registration Details

e2a395c7b2e8bc44c1cda7d6a0bce12f

DHA00601837102

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

Oct 24, 2007

Oct 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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