Taiwan FDA registration 0f241dc4bd1f55525313d08b5018017d
"Mitoyo" obstetrics and gynecology examination table
TW: "三豐"婦產科檢查台
Taiwan·Risk Class 2·BENQ MEDICAL TECHNOLOGY CORPORATION·Registered Sep 30, 2005 – Sep 30, 2015CancelledRegistration details
- Analysis ID
- 0f241dc4bd1f55525313d08b5018017d
- Customs Code
- DHY00500151303
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)
- l Obstetrics and Gynecology
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 30, 2005
- Expiry Date
- Sep 30, 2015
- 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" obstetrics and gynecology examination table in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f241dc4bd1f55525313d08b5018017d and manufactured by BENQ MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is BENQ MEDICAL TECHNOLOGY CORPORATION.
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