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"Meridian" ophthalmic chrome chromium laser - Taiwan Registration 6b819966d4b64631253a41cd354b0885

Access comprehensive regulatory information for "Meridian" ophthalmic chrome chromium laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b819966d4b64631253a41cd354b0885 and manufactured by MERIDIAN AG. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT 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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6b819966d4b64631253a41cd354b0885
Registration Details
Taiwan FDA Registration: 6b819966d4b64631253a41cd354b0885
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Device Details

"Meridian" ophthalmic chrome chromium laser
TW: โ€œ็พŽๅˆฉ่ฟชๆฉโ€ ็œผ็ง‘้Šฃ้›…้‰ป้›ทๅฐ„
Risk Class 2

Registration Details

6b819966d4b64631253a41cd354b0885

DHA00601886106

Company Information

Switzerland

Product Details

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

M Ophthalmology

M.4392 ๅพŒๅ›Šๅˆ‡้™ค็”จNd:YAG้›ทๅฐ„

import

Dates and Status

May 15, 2008

May 15, 2023