Taiwan FDA registration 42df5139e5735675b8c7ce661d81c351
"Marscreen" Anti-Spermatozoa Antibody Test (Non-Sterile)
TW: "馬司可玲" 精蟲免疫抗體檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·SCOPESCREEN·Registered Oct 12, 2020 – Oct 12, 2025ExpiredRegistration details
- Analysis ID
- 42df5139e5735675b8c7ce661d81c351
- License Form
- Ministry of Health Medical Device Import No. 022020
- Customs Code
- DHA09402202001
Company information
- Manufacturer
- SCOPESCREEN
- Manufacturer Country
- United States
- Authorized Representative
- BioChain Co., Ltd.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Human Whole Plasma or Serum Immunoassay System (C.5700)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5700 Human whole plasma or serum immunoassay system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 12, 2020
- Expiry Date
- Oct 12, 2025
About this record
Access comprehensive regulatory information for "Marscreen" Anti-Spermatozoa Antibody Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42df5139e5735675b8c7ce661d81c351 and manufactured by SCOPESCREEN. The authorized representative in Taiwan is BioChain Co., 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