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"Priglai" eye laser probe - Taiwan Registration fd7338d99c07e6efd83555937026f609

Access comprehensive regulatory information for "Priglai" eye laser probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd7338d99c07e6efd83555937026f609 and manufactured by Peregrine Surgical Ltd.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.

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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fd7338d99c07e6efd83555937026f609
Registration Details
Taiwan FDA Registration: fd7338d99c07e6efd83555937026f609
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Device Details

"Priglai" eye laser probe
TW: โ€œๆ™ฎ็‘žๆ ผ่Šโ€็œผ็”จ้›ทๅฐ„ๆŽข้‡
Risk Class 2

Registration Details

fd7338d99c07e6efd83555937026f609

DHA00602459500

Company Information

United States

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

Apr 23, 2013

Apr 23, 2028