Taiwan FDA registration 428ba437ecb350ed68fb2046ca576e53
"Jingxuan" pulsed light meter
TW: “敬煇”脈衝光儀
Registration details
- Analysis ID
- 428ba437ecb350ed68fb2046ca576e53
- Customs Code
- DHY00500219609
Company information
- Manufacturer
- TAIEX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIEX CO., LTD.
Product details
- Intended Use
- Hair removal.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4810 Lasers for general surgical, orthopaedic and dermatological use
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 26, 2007
- Expiry Date
- Apr 26, 2027
About this record
Access comprehensive regulatory information for "Jingxuan" pulsed light meter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 428ba437ecb350ed68fb2046ca576e53 and manufactured by TAIEX CO., LTD.. The authorized representative in Taiwan is TAIEX 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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