Taiwan FDA registration 28ab55db641be5102ff1eab05bf246a0

"Deca" three-vitality infrared laser treatment instrument

TW: “德卡”三活力紅外線雷射治療儀

Taiwan·Risk Class 2·DEKA M.E.L.A. S.R.L.·Registered Mar 28, 2007 – Mar 28, 2017Cancelled

Registration details

Analysis ID: 28ab55db641be5102ff1eab05bf246a0
Customs Code: DHA00601796704

Company information

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

Product details

Intended Use: It temporarily improves local blood circulation and relieves muscle pain and stiffness.
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: Mar 28, 2007
Expiry Date: Mar 28, 2017
Cancellation Date: Dec 20, 2019

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Deca" three-vitality infrared laser treatment instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28ab55db641be5102ff1eab05bf246a0 and manufactured by DEKA M.E.L.A. S.R.L.. The authorized representative in Taiwan is NEOASIA LTD..

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