Taiwan FDA registration 14df600cd09f36a788e0758421942401
"Episi" Manual Orthopaedic Surgical Instruments (Non-sterilized)
TW: "愛派司" 手動式骨科手術器械(未滅菌)
Taiwan·Risk Class 1·A PLUS BIOTECHNOLOGY CO., LTD.·Registered Oct 30, 2024 – Oct 30, 2029ActiveRegistration details
- Analysis ID
- 14df600cd09f36a788e0758421942401
Company information
- Manufacturer
- A PLUS BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A PLUS BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification scope of manual orthopedic surgical instruments (N.4540) in the management measures for the classification and grading of medical devices.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Oct 30, 2024
- Expiry Date
- Oct 30, 2029
About this record
Access comprehensive regulatory information for "Episi" Manual Orthopaedic Surgical Instruments (Non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 14df600cd09f36a788e0758421942401 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY CO., LTD..
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