Taiwan FDA registration 36f5d4af74bbf665161f3f3fbd712d77
"Mitoyo" shadowless surgical light
TW: “三豐”無影外科手術燈
Taiwan·Risk Class 2·BENQ MEDICAL TECHNOLOGY CORPORATION·Registered Jul 19, 2011 – Jul 19, 2016CancelledRegistration details
- Analysis ID
- 36f5d4af74bbf665161f3f3fbd712d77
- Customs Code
- DHY00500335001
Company information
- Manufacturer
- BENQ MEDICAL TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4580 Surgical lamp
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 19, 2011
- Expiry Date
- Jul 19, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Mitoyo" shadowless 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 36f5d4af74bbf665161f3f3fbd712d77 and manufactured by BENQ MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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