Taiwan FDA registration 35e57ccf428cbed818a11f79e8aabd15
Trimurella Wicker Test Kit (Unsterilized)
TW: 銳盟 威克絲沙門氏桿菌檢測套組(未滅菌)
Registration details
- Analysis ID
- 35e57ccf428cbed818a11f79e8aabd15
- Customs Code
- DHA04400074300
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- Rapid latex agglutination to detect the serotype of Salmonella.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3550 沙門氏菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2005
- Expiry Date
- Oct 04, 2025
About this record
Access comprehensive regulatory information for Trimurella Wicker 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 35e57ccf428cbed818a11f79e8aabd15 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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