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"Ruineng " Ruiweishi artificial vitreous - Taiwan Registration f5bd37b29475bd96f9f95abceaac8675

Access comprehensive regulatory information for "Ruineng " Ruiweishi 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 f5bd37b29475bd96f9f95abceaac8675 and manufactured by RAYNER INTRAOCULAR LENSES LTD.. The authorized representative in Taiwan is UNITED MEDICAL INC..

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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f5bd37b29475bd96f9f95abceaac8675
Registration Details
Taiwan FDA Registration: f5bd37b29475bd96f9f95abceaac8675
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Device Details

"Ruineng " Ruiweishi artificial vitreous
TW: โ€œ้Šณ่ƒฝโ€็‘žๅจ่ฆ–ไบบๅทฅ็Žป็’ƒ้ซ”
Risk Class 3
Cancelled

Registration Details

f5bd37b29475bd96f9f95abceaac8675

DHA00601850602

Company Information

United Kingdom

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

Dec 19, 2007

Dec 19, 2022

Apr 12, 2024

Cancellation Information

Logged out

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