Taiwan FDA registration 99843fd752ef1c357f445c80c2069b66

"Deca" Smartwave laser system

TW: “德卡”思媚麗波雷射系統

Taiwan·Risk Class 2·DEKA M.E.L.A. S.R.L.·Registered Jul 18, 2007 – Jul 18, 2027Active

Registration details

Analysis ID: 99843fd752ef1c357f445c80c2069b66
Customs Code: DHA00601817005

Company information

Manufacturer: DEKA M.E.L.A. S.R.L.
Manufacturer Country: Italy
Authorized Representative: NEOASIA LTD.

Product details

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: import

Dates and status

Registration Date: Jul 18, 2007
Expiry Date: Jul 18, 2027

About this record

Access comprehensive regulatory information for "Deca" Smartwave 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 99843fd752ef1c357f445c80c2069b66 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA 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.