Taiwan FDA registration 010936d239ce6f45b1a1c532075fa210
“CHUNGWOO” CONTLEX HIGH INTENSITY FOCUSED ULTRASOUND (HIFU)
TW: “青友”康提超音波治療儀
Taiwan·Risk Class 2·MD·Chungwoo Co., Ltd·Registered Feb 09, 2020 – Feb 09, 2025ExpiredRegistration details
- Analysis ID
- 010936d239ce6f45b1a1c532075fa210
- License Form
- Ministry of Health Medical Device Import No. 033188
- Customs Code
- DHA05603318804
Company information
- Manufacturer
- Chungwoo Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- K2 INTERNATIONAL MEDICAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4590 Focused Ultrasound Stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 09, 2020
- Expiry Date
- Feb 09, 2025
About this record
Access comprehensive regulatory information for “CHUNGWOO” CONTLEX HIGH INTENSITY FOCUSED ULTRASOUND (HIFU) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 010936d239ce6f45b1a1c532075fa210 and manufactured by Chungwoo Co., Ltd. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices