Taiwan FDA registration d028aea73f75ffebc5c95a8e62b26772
Cybernet dual ultrasonic lithotripsy system
TW: 賽柏網雙重超音波碎石系統
Taiwan·Risk Class 2·Gyrus ACMI, Inc.·Registered Dec 03, 2012 – Dec 03, 2027ActiveRegistration details
- Analysis ID
- d028aea73f75ffebc5c95a8e62b26772
- Customs Code
- DHA00602421602
Company information
- Manufacturer
- Gyrus ACMI, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- YUAN LI INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.4480 電動液壓碎石儀
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Dec 03, 2012
- Expiry Date
- Dec 03, 2027
About this record
Access comprehensive regulatory information for Cybernet dual ultrasonic lithotripsy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d028aea73f75ffebc5c95a8e62b26772 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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