Taiwan FDA registration 563d05f79f7e4fd7dc8fc3759c24da9f
"Love Fast" Axus Carbon Monoxide Test Analyzer (Unsterilized)
TW: “愛快發”艾佛克斯一氧化碳試驗分析儀 (未滅菌)
Taiwan·Risk Class 1·Accriva Diagnostics Inc.·Registered Jul 30, 2019 – Jul 30, 2029ActiveRegistration details
- Analysis ID
- 563d05f79f7e4fd7dc8fc3759c24da9f
- Customs Code
- DHA09402069701
Company information
- Manufacturer
- Accriva Diagnostics Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Carbon Monoxide Test System (A.3220)" of the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.3220 Carbon Monoxide Test System
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jul 30, 2019
- Expiry Date
- Jul 30, 2029
About this record
Access comprehensive regulatory information for "Love Fast" Axus Carbon Monoxide Test Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 563d05f79f7e4fd7dc8fc3759c24da9f and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen Taiwan Limited.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices