Taiwan FDA registration c2f2450207b15b03c96e636ce47da594
“BIOPRO”Go-EZ Cannulated Screw System
TW: “拜歐博”簡易中空骨釘系統
Taiwan·Risk Class 2·MD·BIOPRO, INC.·Registered Feb 13, 2017 – Feb 13, 2027ActiveRegistration details
- Analysis ID
- c2f2450207b15b03c96e636ce47da594
- License Form
- Ministry of Health Medical Device Import No. 029365
- Customs Code
- DHA05602936501
Company information
- Manufacturer
- BIOPRO, INC.
- Manufacturer Country
- United States
- Authorized Representative
- EULOGIUMS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3040 Smooth or threaded metal bone fixation
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 13, 2017
- Expiry Date
- Feb 13, 2027
About this record
Access comprehensive regulatory information for “BIOPRO”Go-EZ Cannulated Screw System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2f2450207b15b03c96e636ce47da594 and manufactured by BIOPRO, INC.. The authorized representative in Taiwan is EULOGIUMS CO., LTD..
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