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"ZEISS" ophthalmic laser system - Taiwan Registration ddf42a6dcf0c37bc0a1b956bde359af6

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 ddf42a6dcf0c37bc0a1b956bde359af6 and manufactured by CARL ZEISS MEDITEC AG. The authorized representative in Taiwan is Carl Zeiss Co., Ltd. Taipei Branch.

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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ddf42a6dcf0c37bc0a1b956bde359af6
Registration Details
Taiwan FDA Registration: ddf42a6dcf0c37bc0a1b956bde359af6
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Device Details

"ZEISS" ophthalmic laser system
TW: โ€œ่”กๅธโ€ ็œผ็ง‘้†ซ็™‚้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

ddf42a6dcf0c37bc0a1b956bde359af6

DHA05603675706

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

M Ophthalmology

M.4390 ็œผ็ง‘้›ทๅฐ„่ฃ็ฝฎ

import

Dates and Status

Nov 14, 2023

Nov 14, 2028

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