Taiwan FDA registration 461a07517a167048632b13e5b950552e
“Gyrus ACMI” E-Z Grip Guidewire Torque Device
TW: “吉洛氏 艾斯米”簡易導引線扭矩裝置
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered Dec 25, 2014 – Dec 25, 2024ExpiredRegistration details
- Analysis ID
- 461a07517a167048632b13e5b950552e
- License Form
- Ministry of Health Medical Device Import No. 026876
- Customs Code
- DHA05602687608
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-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 25, 2014
- Expiry Date
- Dec 25, 2024
About this record
Access comprehensive regulatory information for “Gyrus ACMI” E-Z Grip Guidewire Torque Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 461a07517a167048632b13e5b950552e and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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