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Dr. "Dika" Arnold's non-invasive treatment device - Taiwan Registration 748dcc1ac82a2d1af9bb5b8fd62a03d7

Access comprehensive regulatory information for Dr. "Dika" Arnold's non-invasive treatment device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 748dcc1ac82a2d1af9bb5b8fd62a03d7 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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748dcc1ac82a2d1af9bb5b8fd62a03d7
Registration Details
Taiwan FDA Registration: 748dcc1ac82a2d1af9bb5b8fd62a03d7
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Device Details

Dr. "Dika" Arnold's non-invasive treatment device
TW: โ€œ็‹„ๅกโ€ ้˜ฟ่ซพๅšๅฃซ้žไพตๅ…ฅๅผๆฒป็™‚่ฃ็ฝฎ
Risk Class 2

Registration Details

748dcc1ac82a2d1af9bb5b8fd62a03d7

DHA05603711000

Company Information

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.5320 ้žๆคๅ…ฅๅผ้›ปๅญๆŽ’ๅฐฟ่‡ชๅˆถ่ฃ็ฝฎ

Contract manufacturing;; input

Dates and Status

Mar 11, 2024

Mar 11, 2029