Taiwan FDA registration 1ed8359b07aa2c9a97c8756f22466db5
"Ekia" ultrasound therapy device
TW: “以基亞”超音波治療儀
Taiwan·Risk Class 3·IGEA S.P.A·Registered Dec 25, 2009 – Dec 25, 2014CancelledRegistration details
- Analysis ID
- 1ed8359b07aa2c9a97c8756f22466db5
- Customs Code
- DHA00602051301
Company information
- Manufacturer
- IGEA S.P.A
- Manufacturer Country
- Italy
- Authorized Representative
- Yajin International Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5300 超音波透熱治療儀
- Import Information
- import
Dates and status
- Registration Date
- Dec 25, 2009
- Expiry Date
- Dec 25, 2014
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ekia" ultrasound 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 1ed8359b07aa2c9a97c8756f22466db5 and manufactured by IGEA S.P.A. The authorized representative in Taiwan is Yajin International Limited.
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