Taiwan FDA registration fd92e5b9f1dbf6a7f7dce1d432b1c128
"Otaka" manual instrument for general surgery (unsterilized)
TW: “大高”一般手術用手動式器械(未滅菌)
Taiwan·Risk Class 1·TAKASAGO MEDICAL INDUSTRY CO., LTD.·Registered Sep 17, 2012 – Sep 17, 2022CancelledRegistration details
- Analysis ID
- fd92e5b9f1dbf6a7f7dce1d432b1c128
- Customs Code
- DHA04401217301
Company information
- Manufacturer
- TAKASAGO MEDICAL INDUSTRY CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- import
Dates and status
- Registration Date
- Sep 17, 2012
- Expiry Date
- Sep 17, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Otaka" manual instrument for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fd92e5b9f1dbf6a7f7dce1d432b1c128 and manufactured by TAKASAGO MEDICAL INDUSTRY CO., LTD.. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
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