Taiwan FDA registration cc9542a9bdee6951693d54608b4309b2
“Surgi” Spino Balloon Kyphoplasty Balloon Catheter System
TW: “舒吉”球囊椎體成形術系統
Taiwan·Risk Class 2·MD·SURGI BIO CO., LTD.·Registered Nov 22, 2017 – Nov 22, 2027ActiveRegistration details
- Analysis ID
- cc9542a9bdee6951693d54608b4309b2
- License Form
- Ministry of Health Medical Device Import No. 030560
- Customs Code
- DHA05603056009
Company information
- Manufacturer
- SURGI BIO CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SUMMIT BIOMED. 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)
- N9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 22, 2017
- Expiry Date
- Nov 22, 2027
About this record
Access comprehensive regulatory information for “Surgi” Spino Balloon Kyphoplasty Balloon Catheter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc9542a9bdee6951693d54608b4309b2 and manufactured by SURGI BIO CO., LTD.. The authorized representative in Taiwan is SUMMIT BIOMED. CO., LTD..
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