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“Surgi” Spino Balloon Kyphoplasty Balloon Catheter System - Taiwan Registration cc9542a9bdee6951693d54608b4309b2

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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Registration Details
Taiwan FDA Registration: cc9542a9bdee6951693d54608b4309b2
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Device Details

“Surgi” Spino Balloon Kyphoplasty Balloon Catheter System
TW: “舒吉”球囊椎體成形術系統
Risk Class 2
MD

Registration Details

cc9542a9bdee6951693d54608b4309b2

Ministry of Health Medical Device Import No. 030560

DHA05603056009

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N9999 Other

Imported from abroad

Dates and Status

Nov 22, 2017

Nov 22, 2027