Taiwan FDA registration c0f66def5a078a16a87b28b3aef3a60f
"Remon" rotavirus latex test kit (unsterilized)
TW: "銳盟"輪狀病毒乳膠檢測套組(未滅菌)
Registration details
- Analysis ID
- c0f66def5a078a16a87b28b3aef3a60f
- Customs Code
- DHA04400343902
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- Rapid latex agglutination assay for rotavirus or other antigens in human samples.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3405 Poliomyelitis virus serum reagent
- Import Information
- import
Dates and status
- Registration Date
- Apr 04, 2006
- Expiry Date
- Apr 04, 2026
About this record
Access comprehensive regulatory information for "Remon" rotavirus latex test kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0f66def5a078a16a87b28b3aef3a60f and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY 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.
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