Taiwan FDA registration f0eaf195cec9783a6325e15bbb886e72
"Medispek" Radios Spike External Shock Wave Therapy Instrument
TW: “麥迪斯派克”雷迪歐斯派克體外震波治療儀
Taiwan·Risk Class 3·MEDISPEC LTD.·Registered Nov 04, 2010 – Nov 04, 2025ExpiredRegistration details
- Analysis ID
- f0eaf195cec9783a6325e15bbb886e72
- Customs Code
- DHA00602163701
Company information
- Manufacturer
- MEDISPEC LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SHARPMED INSTRUMENTS 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
- 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". input
Dates and status
- Registration Date
- Nov 04, 2010
- Expiry Date
- Nov 04, 2025
About this record
Access comprehensive regulatory information for "Medispek" Radios Spike External Shock Wave Therapy Instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f0eaf195cec9783a6325e15bbb886e72 and manufactured by MEDISPEC LTD.. The authorized representative in Taiwan is SHARPMED INSTRUMENTS CO., LTD..
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