"Kendela" holographic super-picosecond laser system
Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Mar 06, 2021 – Mar 06, 2026Expired- Analysis ID
- b71b49495c3a693310fa895845da6305
- Customs Code
- DHA05603425103
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- DYNAMIC MEDICAL TECHNOLOGIES INC.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Contract manufacturing;; input
- Registration Date
- Mar 06, 2021
- Expiry Date
- Mar 06, 2026
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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.