Taiwan FDA registration dd47e68e834ced60c601ac4c764219c3
"Esme" urological endoscopic accessory removal mesh series
TW: "艾斯美"泌尿外科內視鏡附件取出網系列
Taiwan·Risk Class 1·ACMI CORPORATION·Registered Nov 03, 2005 – Nov 03, 2010CancelledRegistration details
- Analysis ID
- dd47e68e834ced60c601ac4c764219c3
- Customs Code
- DHA04400171806
Company information
- Manufacturer
- ACMI CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- SHARPMED INSTRUMENTS CO., LTD.
Product details
- Intended Use
- A cystoscope is inserted to pick up and remove stones from the ureter.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.4680 輸尿管結石移除器
- Import Information
- import
Dates and status
- Registration Date
- Nov 03, 2005
- Expiry Date
- Nov 03, 2010
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Esme" urological endoscopic accessory removal mesh series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd47e68e834ced60c601ac4c764219c3 and manufactured by ACMI CORPORATION. The authorized representative in Taiwan is SHARPMED INSTRUMENTS CO., LTD..
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