Taiwan FDA registration aaea4fd9690a97d2923aa42ca5ff37a6
"Digeou" Interlet New Generation Treatment System
TW: “帝傑歐” 因特列特新世代治療系統
Taiwan·Risk Class 2·DJO France S.A.S;; South Dakota Partners, Inc.·Registered Oct 15, 2021 – Oct 15, 2026ActiveRegistration details
- Analysis ID
- aaea4fd9690a97d2923aa42ca5ff37a6
- Customs Code
- DHA05603487604
Company information
- Manufacturer
- DJO France S.A.S;; South Dakota Partners, Inc.
- Manufacturer Country
- France;;United States
- Authorized Representative
- CONTINUOUS INSTRUMENT 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.5860 超音波及肌肉刺激器;; O.5500 紅外線燈
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Oct 15, 2021
- Expiry Date
- Oct 15, 2026
About this record
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..
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