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"Zeiss" excimer laser and accessories - Taiwan Registration da8742d00ff2741fc10c155866337f20

Access comprehensive regulatory information for "Zeiss" excimer laser and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number da8742d00ff2741fc10c155866337f20 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. 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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da8742d00ff2741fc10c155866337f20
Registration Details
Taiwan FDA Registration: da8742d00ff2741fc10c155866337f20
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Device Details

"Zeiss" excimer laser and accessories
TW: โ€œ่”กๅธโ€ๆบ–ๅˆ†ๅญ้›ทๅฐ„ๅ„€ๅŠ้…ไปถ
Risk Class 3

Registration Details

da8742d00ff2741fc10c155866337f20

DHA05602642501

Company Information

Germany

Product Details

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

M Ophthalmology

M.0001 ็œผ็ง‘็”จๆบ–ๅˆ†ๅญ้›ทๅฐ„็ณป็ตฑ

import

Dates and Status

Aug 06, 2014

Aug 06, 2024