Taiwan FDA registration 34aed621da7076f5c16b09677ff65935

“THUNDERTIGER” Orthopedic Extracorporeal Shock Wave System and Accessories

TW: “雷虎”骨科用體外震波治療儀及其附件

Taiwan·Risk Class 3·MD·THUNDER TIGER CORPORATION·Registered Nov 24, 2022 – Nov 24, 2027Active

Registration details

Analysis ID: 34aed621da7076f5c16b09677ff65935
License Form: Ministry of Health Medical Device Manufacturing No. 007707

Company information

Manufacturer: THUNDER TIGER CORPORATION
Manufacturer Country: Taiwan, Province of China
Authorized Representative: THUNDER TIGER CORPORATION

Product details

Intended Use: Details are as detailed as approved Chinese instructions
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N0001 Extracorporeal shock wave system for orthopedics
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Nov 24, 2022
Expiry Date: Nov 24, 2027

About this record

Access comprehensive regulatory information for “THUNDERTIGER” Orthopedic Extracorporeal Shock Wave System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 34aed621da7076f5c16b09677ff65935 and manufactured by THUNDER TIGER CORPORATION. The authorized representative in Taiwan is THUNDER TIGER CORPORATION.

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