Taiwan FDA registration fbeabeb4bca224fa766e0dcfb5feb6f2
"Akon" ovulation (urine) testing system (unsterilized)
TW: "艾康"排卵(尿液)測試系統(未滅菌)
Taiwan·Risk Class 1·ACON BIOTECH (HANGZHOU) CO., LTD.·Registered Apr 13, 2011 – Apr 13, 2016CancelledRegistration details
- Analysis ID
- fbeabeb4bca224fa766e0dcfb5feb6f2
- Customs Code
- DHA04600133506
Company information
- Manufacturer
- ACON BIOTECH (HANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- MIN JIER FIRM
Product details
- Intended Use
- Limited to the first level identification range of the "luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- import
Dates and status
- Registration Date
- Apr 13, 2011
- Expiry Date
- Apr 13, 2016
- Cancellation Date
- Aug 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Akon" ovulation (urine) testing system (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fbeabeb4bca224fa766e0dcfb5feb6f2 and manufactured by ACON BIOTECH (HANGZHOU) CO., LTD.. The authorized representative in Taiwan is MIN JIER FIRM.
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