Taiwan FDA registration f7cbd379b5fc892d6c7b98c1ceb9dde1
"Draida" clinical sample (unsterilized)
TW: "德芮達" 臨床用樣板 (未滅菌)
Taiwan·Risk Class 1·DETEKT TECHNOLOGY INC.·Registered Mar 23, 2018 – Mar 23, 2028ActiveRegistration details
- Analysis ID
- f7cbd379b5fc892d6c7b98c1ceb9dde1
Company information
- Manufacturer
- DETEKT TECHNOLOGY INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DETEKT TECHNOLOGY INC.
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;; 國產
Dates and status
- Registration Date
- Mar 23, 2018
- Expiry Date
- Mar 23, 2028
About this record
Access comprehensive regulatory information for "Draida" clinical sample (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7cbd379b5fc892d6c7b98c1ceb9dde1 and manufactured by DETEKT TECHNOLOGY INC.. The authorized representative in Taiwan is DETEKT TECHNOLOGY INC..
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