Taiwan FDA registration fb3c53dd13b5f7526109542d6926824a
"Kindy" scope and its accessories (unsterilized)
TW: “金蒂”檢查鏡及其附件(未滅菌)
Taiwan·Risk Class 1·TIDI PRODUCTS, LLC·Registered May 24, 2012 – May 24, 2022CancelledRegistration details
- Analysis ID
- fb3c53dd13b5f7526109542d6926824a
- Customs Code
- DHA04401174400
Company information
- Manufacturer
- TIDI PRODUCTS, LLC
- Manufacturer Country
- United States
- Authorized Representative
- KING DAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.1800 Inspection Scopes and Annexes
- Import Information
- import
Dates and status
- Registration Date
- May 24, 2012
- Expiry Date
- May 24, 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 "Kindy" scope and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fb3c53dd13b5f7526109542d6926824a and manufactured by TIDI PRODUCTS, LLC. The authorized representative in Taiwan is KING DAY CO., LTD..
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