Taiwan FDA registration f1f12c87b8399881e45f798167137510
"Difu Xindis" Provisional Plate (Extinction/Unindestructible)
TW: "帝富信迪思" 臨床用樣板(滅菌/未滅菌)
Taiwan·Risk Class 1·SYNTHES GMBH·Registered May 29, 2024 – May 29, 2029ActiveRegistration details
- Analysis ID
- f1f12c87b8399881e45f798167137510
- Customs Code
- DHA09402349106
Company information
- Manufacturer
- SYNTHES GMBH
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Clinical Model (N.4800)" for the classification and grading management measures of medical devices.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4800 Sample plate for clinical use
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- May 29, 2024
- Expiry Date
- May 29, 2029
About this record
Access comprehensive regulatory information for "Difu Xindis" Provisional Plate (Extinction/Unindestructible) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f1f12c87b8399881e45f798167137510 and manufactured by SYNTHES GMBH. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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