Taiwan FDA registration 86e92ccb5bef7279961386d169c6e21a
Quick and easy pregnancy test products
TW: 快易準驗孕產品
Registration details
- Analysis ID
- 86e92ccb5bef7279961386d169c6e21a
- Customs Code
- DHA00601715504
Company information
- Manufacturer
- UNOTECH DIAGNOSTICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Shengpu International Limited
Product details
- Intended Use
- Placental hormones in human urine are measured to detect pregnancy at an early stage.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- import
Dates and status
- Registration Date
- Jun 27, 2006
- Expiry Date
- Jun 27, 2011
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Quick and easy pregnancy test products in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 86e92ccb5bef7279961386d169c6e21a and manufactured by UNOTECH DIAGNOSTICS, INC.. The authorized representative in Taiwan is Shengpu International 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