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"Digeou" Interlet New Generation Treatment System - Taiwan Registration aaea4fd9690a97d2923aa42ca5ff37a6

Access comprehensive regulatory information for "Digeou" Interlet New Generation Treatment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aaea4fd9690a97d2923aa42ca5ff37a6 and manufactured by DJO France S.A.S;; South Dakota Partners, Inc.. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT 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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aaea4fd9690a97d2923aa42ca5ff37a6
Registration Details
Taiwan FDA Registration: aaea4fd9690a97d2923aa42ca5ff37a6
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Device Details

"Digeou" Interlet New Generation Treatment System
TW: โ€œๅธๅ‚‘ๆญโ€ ๅ› ็‰นๅˆ—็‰นๆ–ฐไธ–ไปฃๆฒป็™‚็ณป็ตฑ
Risk Class 2

Registration Details

aaea4fd9690a97d2923aa42ca5ff37a6

DHA05603487604

Company Information

France;;United States

Product Details

Details are as detailed as approved Chinese instructions

o Physical Medical Sciences

O.5860 ่ถ…้ŸณๆณขๅŠ่‚Œ่‚‰ๅˆบๆฟ€ๅ™จ;; O.5500 ็ด…ๅค–็ทš็‡ˆ

Input;; Contract manufacturing

Dates and Status

Oct 15, 2021

Oct 15, 2026