Taiwan FDA registration 4a8389a4deeb5ff746368fb01b34b081
BIONOX Injectable Artificial Bone Filler Dispenser Set (Sterilized)
TW: 保諾士 可注射型人工骨填充物分配器組 (滅菌)
Taiwan·Risk Class 1·SHINEO TECHNOLOGY CO., LTD.·Registered Mar 28, 2016 – Mar 28, 2026ExpiredRegistration details
- Analysis ID
- 4a8389a4deeb5ff746368fb01b34b081
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHINEO TECHNOLOGY CO., 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;; 國產
Dates and status
- Registration Date
- Mar 28, 2016
- Expiry Date
- Mar 28, 2026
About this record
Access comprehensive regulatory information for BIONOX Injectable Artificial Bone Filler Dispenser Set (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4a8389a4deeb5ff746368fb01b34b081 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..
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