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Taiwan FDA registration 2b71638fe654d51babbe0fafa6e9ad29

"Dika" magnetic wave stimulator

TW: “狄卡” 磁波刺激器
Taiwan flagTaiwan·Risk Class 2·EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.·Registered Dec 01, 2021 – Dec 01, 2026Active
Registration details
Analysis ID
2b71638fe654d51babbe0fafa6e9ad29
Customs Code
DHA05603504607
Company information
Manufacturer
EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.
Manufacturer Country
Italy
Authorized Representative
K&C MEDICAL CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5850 5850.
Import Information
import
Dates and status
Registration Date
Dec 01, 2021
Expiry Date
Dec 01, 2026
About this record

Access comprehensive regulatory information for "Dika" magnetic wave stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b71638fe654d51babbe0fafa6e9ad29 and manufactured by EL.EN. S.p.A.;; DEKA M.E.L.A. S.r.l.. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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