Taiwan FDA registration 0656fd15413c86ac69cad9762637e987
"Apas" Universal Osteotomy Guidance Plate System (Unsterilized)
TW: “愛派司”通用型截骨手術導引板系統(未滅菌)
Taiwan·Risk Class 1·A PLUS BIOTECHNOLOGY CO., LTD.·Registered Dec 04, 2018 – Dec 04, 2028ActiveRegistration details
- Analysis ID
- 0656fd15413c86ac69cad9762637e987
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
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- 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
- Dec 04, 2018
- Expiry Date
- Dec 04, 2028
About this record
Access comprehensive regulatory information for "Apas" Universal Osteotomy Guidance Plate System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0656fd15413c86ac69cad9762637e987 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY CO., LTD..
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