Taiwan FDA registration cd09150b4c1435360e809d30677b146c
"AMTAI" Medical Examination Light (NON-STERILE)
TW: "銨鈦" 醫用檢查燈 (未滅菌)
Taiwan·Risk Class 1·MD·AMTAI MEDICAL EQUIPMENT, INC.·Registered Oct 19, 2016 – Oct 19, 2021ExpiredRegistration details
- Analysis ID
- cd09150b4c1435360e809d30677b146c
- License Form
- Ministry of Health Medical Device Import No. 017096
- Customs Code
- DHA09401709601
Company information
- Manufacturer
- AMTAI MEDICAL EQUIPMENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WEI-JUN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Light Source for Optical Fiber Dentistry (F.4620)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4620 Light source for photofiber dentistry
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 19, 2016
- Expiry Date
- Oct 19, 2021
About this record
Access comprehensive regulatory information for "AMTAI" Medical Examination Light (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd09150b4c1435360e809d30677b146c and manufactured by AMTAI MEDICAL EQUIPMENT, INC.. The authorized representative in Taiwan is WEI-JUN INSTRUMENT CO., LTD..
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