Taiwan FDA registration 748dcc1ac82a2d1af9bb5b8fd62a03d7

Dr. "Dika" Arnold's non-invasive treatment device

TW: “狄卡” 阿諾博士非侵入式治療裝置

Taiwan·Risk Class 2·DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.·Registered Mar 11, 2024 – Mar 11, 2029Active

Registration details

Analysis ID: 748dcc1ac82a2d1af9bb5b8fd62a03d7
Customs Code: DHA05603711000

Company information

Manufacturer: DEKA M.E.L.A. S.r.l.;; EL.EN. S.p.A.
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): H Gastroenterology and urology
Product Type (Level 2): H.5320 非植入式電子排尿自制裝置
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Mar 11, 2024
Expiry Date: Mar 11, 2029

About this record

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..

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