Taiwan FDA registration 88f8ab0b1ac54225cf8331b9add714c0
"Episi" Manual Orthopedic Surgical Instruments (Sterilized)
TW: "愛派司" 手動式骨科手術器械(滅菌)
Taiwan·Risk Class 1·A PLUS BIOTECHNOLOGY CO., LTD.·Registered Nov 21, 2024 – Nov 21, 2029ActiveRegistration details
- Analysis ID
- 88f8ab0b1ac54225cf8331b9add714c0
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
- Nov 21, 2024
- Expiry Date
- Nov 21, 2029
About this record
Access comprehensive regulatory information for "Episi" Manual Orthopedic Surgical Instruments (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88f8ab0b1ac54225cf8331b9add714c0 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY CO., LTD..
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