"Kendela" holographic super-picosecond laser system
Taiwan·Risk Class 2·NPA DE MEXICO S. DE R.L. DE C.V.;; Candela Corporation·Registered Jun 03, 2017 – Jun 03, 2027Active- Analysis ID
- f2610acca156dce14ce7e52860c33f87
- Customs Code
- DHA05602987903
- 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
- Jun 03, 2017
- Expiry Date
- Jun 03, 2027
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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 f2610acca156dce14ce7e52860c33f87 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.