Taiwan FDA registration 27532f5f9ce038d2abcf4089e35e8e04
“Fukuda” Patient Monitor
TW: “福田”生理監護儀
Taiwan·Risk Class 2·MD·BRITEMED TECHNOLOGY INC.·Registered May 01, 2019 – May 01, 2024ExpiredRegistration details
- Analysis ID
- 27532f5f9ce038d2abcf4089e35e8e04
- License Form
- Ministry of Health Medical Device Manufacturing No. 006413
Company information
- Manufacturer
- BRITEMED TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BRITEMED TECHNOLOGY INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 01, 2019
- Expiry Date
- May 01, 2024
About this record
Access comprehensive regulatory information for “Fukuda” Patient Monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27532f5f9ce038d2abcf4089e35e8e04 and manufactured by BRITEMED TECHNOLOGY INC.. The authorized representative in Taiwan is BRITEMED TECHNOLOGY INC..
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