Taiwan FDA registration 5ef2ef1b3412395c03928d2d77fa5429
“M.I.Tech” MASON M1 Extracorporeal Shockwave Lithotripter
TW: 摩昇體外震波碎石機
Taiwan·Risk Class 2·MD·M.I. Tech Co., Ltd.·Registered Jun 08, 2023 – Jun 08, 2028ActiveRegistration details
- Analysis ID
- 5ef2ef1b3412395c03928d2d77fa5429
- License Form
- Ministry of Health Medical Device Import No. 036536
- Customs Code
- DHA05603653603
Company information
- Manufacturer
- M.I. Tech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- KUAN FWA MED CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5990 Extracorporeal shock wave lithotripsy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 08, 2023
- Expiry Date
- Jun 08, 2028
About this record
Access comprehensive regulatory information for “M.I.Tech” MASON M1 Extracorporeal Shockwave Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5ef2ef1b3412395c03928d2d77fa5429 and manufactured by M.I. Tech Co., Ltd.. The authorized representative in Taiwan is KUAN FWA MED CO., LTD..
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