Taiwan FDA registration a7e0e7eada9bf5fa955094da420bc382
"Zhengtian" manual osteologic surgical instrument (unsterile)
TW: "正天" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·TIANJIN ZHENGTIAN MEDICAL INSTRUMENT CO., LTD.·Registered Jul 20, 2017 – Jul 20, 2027ActiveRegistration details
- Analysis ID
- a7e0e7eada9bf5fa955094da420bc382
- Customs Code
- DHA09600314800
Company information
- Manufacturer
- TIANJIN ZHENGTIAN MEDICAL INSTRUMENT CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- CHIN BONE TECHNIQUE CORP.
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
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 20, 2017
- Expiry Date
- Jul 20, 2027
About this record
Access comprehensive regulatory information for "Zhengtian" manual osteologic surgical instrument (unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a7e0e7eada9bf5fa955094da420bc382 and manufactured by TIANJIN ZHENGTIAN MEDICAL INSTRUMENT CO., LTD.. The authorized representative in Taiwan is CHIN BONE TECHNIQUE CORP..
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