Taiwan FDA registration 68a3fb3e04bea20085b2fb458c07f000
"BenQ Mitoyo" Medical Inspection Light (Unsterilized)
TW: "明基三豐" 醫用檢查燈 (未滅菌)
Taiwan·Risk Class 1·BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory·Registered Oct 20, 2015 – Oct 20, 2025ExpiredRegistration details
- Analysis ID
- 68a3fb3e04bea20085b2fb458c07f000
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Optical Fiber Dental Light Source (F.4620)" of the Administrative Measures for the Classification and Classification of Medical Devices.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4620 Light source for optical fiber dentistry
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 20, 2015
- Expiry Date
- Oct 20, 2025
About this record
Access comprehensive regulatory information for "BenQ Mitoyo" Medical Inspection Light (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 68a3fb3e04bea20085b2fb458c07f000 and manufactured by BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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