Taiwan FDA registration 58406e5a38b1b56b8ae22d7cfcc01e3b
“NeuLight” Holmium Laser Fibers
TW: “紐萊特”雷射光纖
Taiwan·Risk Class 2·MD·WEINERT Fiber Optics, Inc.·Registered Oct 13, 2023 – Oct 13, 2028ActiveRegistration details
- Analysis ID
- 58406e5a38b1b56b8ae22d7cfcc01e3b
- License Form
- Ministry of Health Medical Device Import No. 036805
- Customs Code
- DHA05603680504
Company information
- Manufacturer
- WEINERT Fiber Optics, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- JIANHE BIO-MEDICAL 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
- Oct 13, 2023
- Expiry Date
- Oct 13, 2028
About this record
Access comprehensive regulatory information for “NeuLight” Holmium Laser Fibers in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58406e5a38b1b56b8ae22d7cfcc01e3b and manufactured by WEINERT Fiber Optics, Inc.. The authorized representative in Taiwan is JIANHE BIO-MEDICAL LTD..
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