Taiwan FDA registration fa7c727bc68229b49644735759550f81
“Gyrus ACMI” Dual Lumen Catheter
TW: “吉洛氏 艾斯米”雙腔導管
Taiwan·Risk Class 2·MD·Gyrus ACMI, Inc.·Registered May 28, 2015 – May 28, 2025ExpiredRegistration details
- Analysis ID
- fa7c727bc68229b49644735759550f81
- License Form
- Ministry of Health Medical Device Import No. 027405
- Customs Code
- DHA05602740500
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)
- H5130 Urinary catheters and their accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2015
- Expiry Date
- May 28, 2025
About this record
Access comprehensive regulatory information for “Gyrus ACMI” Dual Lumen Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa7c727bc68229b49644735759550f81 and manufactured by Gyrus ACMI, Inc.. The authorized representative in Taiwan is YUAN LI INSTRUMENT CO., LTD..
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