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"Deca" Mortex laser - Taiwan Registration f52fefdff1af2279f774839ca22bcd58

Access comprehensive regulatory information for "Deca" Mortex laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f52fefdff1af2279f774839ca22bcd58 and manufactured by DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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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f52fefdff1af2279f774839ca22bcd58
Registration Details
Taiwan FDA Registration: f52fefdff1af2279f774839ca22bcd58
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Device Details

"Deca" Mortex laser
TW: โ€œๅพทๅกโ€ๆ‘ฉ็‰น็ตฒ้›ทๅฐ„
Risk Class 2

Registration Details

f52fefdff1af2279f774839ca22bcd58

DHA05603023205

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

Input;; Contract manufacturing

Dates and Status

Sep 15, 2017

Sep 15, 2027