Taiwan FDA registration 767b274c8e5d5dc5623c59fbe6f8f030
"Situo" multi-force shock wave therapy system and accessories
TW: “思拓”多力震波治療系統與配件
Taiwan·Risk Class 3·STORZ MEDICAL AG·Registered Jan 27, 2014 – Jan 27, 2019CancelledRegistration details
- Analysis ID
- 767b274c8e5d5dc5623c59fbe6f8f030
- Customs Code
- DHA05602577204
Company information
- Manufacturer
- STORZ MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- SHAWHAN BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as the Chinese copy of the approved version. Performance changes: Details are as detailed as the Chinese copy of the approved version, and the following blanks.
- Product Type (Level 1)
- N Orthopedics;; H Gastroenterology and Urology
- Product Type (Level 2)
- N.0001 骨科用體外震波系統;; H.9999 其他
- Import Information
- import
Dates and status
- Registration Date
- Jan 27, 2014
- Expiry Date
- Jan 27, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Situo" multi-force shock wave therapy 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 767b274c8e5d5dc5623c59fbe6f8f030 and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..
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