Taiwan FDA registration b461d1463ef4d569672e43cc563b06ec
“INTRA-LOCK” ReOss Synthetic Biomaterial
TW: “英德樂可”里奧斯合成骨粉
Taiwan·Risk Class 2·MD·INTRA-LOCK INTERNATIONAL, INC.·Registered Jul 02, 2014 – Jul 02, 2024ExpiredRegistration details
- Analysis ID
- b461d1463ef4d569672e43cc563b06ec
- License Form
- Ministry of Health Medical Device Import No. 026322
- Customs Code
- DHA05602632204
Company information
- Manufacturer
- INTRA-LOCK INTERNATIONAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HONG YANG BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3930 Tricalcium phosphate for alveolar bone restoration
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 02, 2014
- Expiry Date
- Jul 02, 2024
About this record
Access comprehensive regulatory information for “INTRA-LOCK” ReOss Synthetic Biomaterial in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b461d1463ef4d569672e43cc563b06ec and manufactured by INTRA-LOCK INTERNATIONAL, INC.. The authorized representative in Taiwan is HONG YANG BIOTECHNOLOGY CO., LTD..
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