Taiwan FDA registration abb94b38dd60b04ddbfd4ddd594e9256
"Kehui" Manual Orthopaedic Surgical Device (Inverted Bacteria)
TW: "科惠" 手動式骨科手術器械(未滅菌)
Taiwan·Risk Class 1·CANWELL MEDICAL CO, LTD.·Registered Dec 26, 2023 – Dec 26, 2028ActiveRegistration details
- Analysis ID
- abb94b38dd60b04ddbfd4ddd594e9256
- Customs Code
- DHA09600486300
Company information
- Manufacturer
- CANWELL MEDICAL CO, LTD.
- Manufacturer Country
- China
- Authorized Representative
- HELE TECHNOLOGY 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;; Input;; Chinese goods
Dates and status
- Registration Date
- Dec 26, 2023
- Expiry Date
- Dec 26, 2028
About this record
Access comprehensive regulatory information for "Kehui" Manual Orthopaedic Surgical Device (Inverted Bacteria) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number abb94b38dd60b04ddbfd4ddd594e9256 and manufactured by CANWELL MEDICAL CO, LTD.. The authorized representative in Taiwan is HELE TECHNOLOGY CO., LTD..
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