Taiwan FDA registration 40cff0ab0beeee78c60452fa9762482e
“AtriCure” AtriClip FLEX LAA Exclusion System
TW: “艾翠科” 弗列斯左心耳閉塞夾系統
Taiwan·Risk Class 2·MD·Atricure, Inc.·Registered Jul 13, 2021 – Jul 13, 2026ExpiredRegistration details
- Analysis ID
- 40cff0ab0beeee78c60452fa9762482e
- License Form
- Ministry of Health Medical Device Import No. 034757
- Customs Code
- DHA05603475709
Company information
- Manufacturer
- Atricure, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 13, 2021
- Expiry Date
- Jul 13, 2026
About this record
Access comprehensive regulatory information for “AtriCure” AtriClip FLEX LAA Exclusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 40cff0ab0beeee78c60452fa9762482e and manufactured by Atricure, Inc.. The authorized representative in Taiwan is ASIA HEALTH CARE CO., LTD..
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