Taiwan FDA registration 4458229e001517283fac098d695e092e
"Svetik" orthopedic shock wave therapy machine
TW: “史威堤克”骨科震波治療機
Taiwan·Risk Class 3·SWITTECH MEDICAL AG·Registered Oct 28, 2010 – Oct 28, 2015CancelledRegistration details
- Analysis ID
- 4458229e001517283fac098d695e092e
- Customs Code
- DHA00602160906
Company information
- Manufacturer
- SWITTECH MEDICAL AG
- Manufacturer Country
- Switzerland
- Authorized Representative
- LITHO MED TRADING CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.0001 骨科用體外震波系統
- Import Information
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Oct 28, 2010
- Expiry Date
- Oct 28, 2015
- Cancellation Date
- Aug 14, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Svetik" orthopedic shock wave therapy machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4458229e001517283fac098d695e092e and manufactured by SWITTECH MEDICAL AG. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..
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