Taiwan FDA registration 6254f021f639ea552d8800280c2dfaee
“BenQ” Surgical Light
TW: “明基三豐”外科手術燈
Taiwan·Risk Class 2·MD·BenQ Mitoyo Medical Equipment Co., Ltd. Guishan Factory·Registered Mar 08, 2022 – Mar 08, 2027ActiveRegistration details
- Analysis ID
- 6254f021f639ea552d8800280c2dfaee
- License Form
- Ministry of Health Medical Device Manufacturing No. 007364
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
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)
- I4580 Surgical light
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 08, 2022
- Expiry Date
- Mar 08, 2027
About this record
Access comprehensive regulatory information for “BenQ” Surgical Light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6254f021f639ea552d8800280c2dfaee 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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