Taiwan FDA registration b3e9f37c5e15aed44e009f3ef4abecbe
"Sindis" bone cement dispenser (sterilized/unsterilized)
TW: "信迪思"骨水泥分配器 (滅菌/未滅菌)
Taiwan·Risk Class 1·SYNTHES GMBH·Registered Jan 16, 2019 – Jan 16, 2029ActiveRegistration details
- Analysis ID
- b3e9f37c5e15aed44e009f3ef4abecbe
- Customs Code
- DHA09402003109
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Bone cement dispenser (N.4200) first level identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4200 Bone cement distributor
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 16, 2019
- Expiry Date
- Jan 16, 2029
About this record
Access comprehensive regulatory information for "Sindis" bone cement dispenser (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b3e9f37c5e15aed44e009f3ef4abecbe and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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