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"Zeiss" ophthalmic laser system - Taiwan Registration e16e74cd8d9cf098b08eff8402d7336c

Access comprehensive regulatory information for "Zeiss" ophthalmic laser system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e16e74cd8d9cf098b08eff8402d7336c and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CARL ZEISS MEDITEC AG, and 4 recent registrations in the same category. 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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e16e74cd8d9cf098b08eff8402d7336c
Registration Details
Taiwan FDA Registration: e16e74cd8d9cf098b08eff8402d7336c
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Device Details

"Zeiss" ophthalmic laser system
TW: "่”กๅธ"็œผ็ง‘้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

e16e74cd8d9cf098b08eff8402d7336c

DHA00601451200

Company Information

Germany

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 26, 2006

May 26, 2021

Sep 23, 2023

Cancellation Information

Logged out

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