Taiwan FDA registration f57097e04c3ecd93652e066de7471d2f
Omnilux System
TW: “歐霓”光療儀
Taiwan·Risk Class 2·MD·GLOBALMED TECHNOLOGIES CO·Registered May 25, 2020 – May 25, 2025ExpiredRegistration details
- Analysis ID
- f57097e04c3ecd93652e066de7471d2f
- License Form
- Ministry of Health Medical Device Import No. 033662
- Customs Code
- DHA05603366206
Company information
- Manufacturer
- GLOBALMED TECHNOLOGIES CO
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN GREEN CROSS CO., LTD.
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)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2020
- Expiry Date
- May 25, 2025
About this record
Access comprehensive regulatory information for Omnilux System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f57097e04c3ecd93652e066de7471d2f and manufactured by GLOBALMED TECHNOLOGIES CO. The authorized representative in Taiwan is TAIWAN GREEN CROSS CO., LTD..
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