Taiwan FDA registration 2d1ab6cdc68195a8403e16b2dc3028d9
"Irek" extracorporeal shock wave therapy device
TW: “伊雷克”體外震波治療儀
Taiwan·Risk Class 3·E.M.S. Electro Medical Systems S.A.;; E.M.S. ELECTRO MEDICAL SYSTEMS S.A.·Registered Jan 14, 2013 – Jan 14, 2028ActiveRegistration details
- Analysis ID
- 2d1ab6cdc68195a8403e16b2dc3028d9
- Customs Code
- DHA00602444109
Company information
- Manufacturer Country
- Switzerland
- Authorized Representative
- MEDEN INTERNATIONAL INC.
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
- import
Dates and status
- Registration Date
- Jan 14, 2013
- Expiry Date
- Jan 14, 2028
About this record
Access comprehensive regulatory information for "Irek" extracorporeal shock wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2d1ab6cdc68195a8403e16b2dc3028d9 and manufactured by E.M.S. Electro Medical Systems S.A.;; E.M.S. ELECTRO MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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