Taiwan FDA registration 74596530fc9ff21fa3f728e90e70b81f
"Difu Xindis" Provisional Sample Plate (Unextinguished)
TW: “帝富信迪思” 臨床用樣板(未滅菌)
Taiwan·Risk Class 1·MEDOS INTERNATIONAL SARL·Registered Sep 04, 2023 – Sep 04, 2028ActiveRegistration details
- Analysis ID
- 74596530fc9ff21fa3f728e90e70b81f
- Customs Code
- DHA09402323300
Company information
- Manufacturer
- MEDOS INTERNATIONAL SARL
- 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 "Clinical Use Model (N.4800) First Level Identification Range".
- 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
- Sep 04, 2023
- Expiry Date
- Sep 04, 2028
About this record
Access comprehensive regulatory information for "Difu Xindis" Provisional Sample Plate (Unextinguished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 74596530fc9ff21fa3f728e90e70b81f and manufactured by MEDOS INTERNATIONAL SARL. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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