Taiwan FDA registration 4cd626759d03eee3c53757ae23be76e1
"Baoer" ovulation test reagent (unsterilized)
TW: "寶兒"排卵測試試劑(未滅菌)
Taiwan·Risk Class 1·IND DIAGNOSTIC INC.·Registered May 28, 2012 – May 28, 2017CancelledRegistration details
- Analysis ID
- 4cd626759d03eee3c53757ae23be76e1
- Customs Code
- DHA04401175607
Company information
- Manufacturer
- IND DIAGNOSTIC INC.
- Manufacturer Country
- Canada
- Authorized Representative
- ELAN ACCESSORIES COMPANY LTD.
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
- May 28, 2012
- Expiry Date
- May 28, 2017
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Baoer" ovulation test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4cd626759d03eee3c53757ae23be76e1 and manufactured by IND DIAGNOSTIC INC.. The authorized representative in Taiwan is ELAN ACCESSORIES COMPANY LTD..
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