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"Kendela" holographic super-picosecond laser system - Taiwan Registration b71b49495c3a693310fa895845da6305

Access comprehensive regulatory information for "Kendela" holographic super-picosecond 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 b71b49495c3a693310fa895845da6305 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation, and 1 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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b71b49495c3a693310fa895845da6305
Registration Details
Taiwan FDA Registration: b71b49495c3a693310fa895845da6305
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Device Details

"Kendela" holographic super-picosecond laser system
TW: โ€œ่‚ฏๅพ—ๆ‹‰โ€ๅ…จๅƒ่ถ…็šฎ็ง’้›ทๅฐ„็ณป็ตฑ
Risk Class 2

Registration Details

b71b49495c3a693310fa895845da6305

DHA05603425103

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

Contract manufacturing;; input

Dates and Status

Mar 06, 2021

Mar 06, 2026

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