Taiwan FDA registration cea61f2797c0c915153d6eeb631f13c8
"Teifu Xin Disi Spine" Manual osteologic surgical instrument (sterile/unsterilized)
TW: "帝富信迪思脊椎" 手動式骨科手術器械 (滅菌/未滅菌)
Taiwan·Risk Class 1·SYNTHES GMBH·Registered Nov 21, 2019 – Nov 21, 2029ActiveRegistration details
- Analysis ID
- cea61f2797c0c915153d6eeb631f13c8
- Customs Code
- DHA09402103002
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 "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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 21, 2019
- Expiry Date
- Nov 21, 2029
About this record
Access comprehensive regulatory information for "Teifu Xin Disi Spine" Manual osteologic surgical instrument (sterile/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cea61f2797c0c915153d6eeb631f13c8 and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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