Taiwan FDA registration 001e087e2dcfa9380eb43ccc39d01226
“EunSung” Clearlight LD 808
TW: “恩尚”二極體雷射
Taiwan·Risk Class 2·MD·EUNSUNG GLOBAL CORP.·Registered Apr 20, 2022 – Apr 20, 2027ActiveRegistration details
- Analysis ID
- 001e087e2dcfa9380eb43ccc39d01226
- License Form
- Ministry of Health Medical Device Import No. 035397
- Customs Code
- DHA05603539700
Company information
- Manufacturer
- EUNSUNG GLOBAL CORP.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MAVIS MEDICAL ENTERPRISE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I4810 Lasers for general surgery, plastic surgery and dermatology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2022
- Expiry Date
- Apr 20, 2027
About this record
Access comprehensive regulatory information for “EunSung” Clearlight LD 808 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 001e087e2dcfa9380eb43ccc39d01226 and manufactured by EUNSUNG GLOBAL CORP.. The authorized representative in Taiwan is MAVIS MEDICAL ENTERPRISE CO., LTD..
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