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"Zeiss" ophthalmic laser system - Taiwan Registration 571f6b9fe49255e6cf09aae9b0efc021

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 571f6b9fe49255e6cf09aae9b0efc021 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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571f6b9fe49255e6cf09aae9b0efc021
Registration Details
Taiwan FDA Registration: 571f6b9fe49255e6cf09aae9b0efc021
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Device Details

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

Registration Details

571f6b9fe49255e6cf09aae9b0efc021

DHA00601660504

Company Information

Germany

Product Details

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

M Ophthalmology

M.4390 ็œผ็ง‘้›ทๅฐ„่ฃ็ฝฎ

import

Dates and Status

May 30, 2006

May 30, 2021

Sep 23, 2023

Cancellation Information

Logged out

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