Taiwan FDA registration b59f72073df2a65928b00f3984f5ca01
"Remon" Proteus suspension staining reagent and Proteus agglutination serum (unsterilized)
TW: "銳盟" 變形桿菌懸浮染色試劑和變形桿菌凝集血清 (未滅菌)
Registration details
- Analysis ID
- b59f72073df2a65928b00f3984f5ca01
- Customs Code
- DHA04400080509
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- Antibodies that detect rickettsia in the human body.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3410 Serum sample of the Bacillus Bacillus
- Import Information
- import
Dates and status
- Registration Date
- Oct 06, 2005
- Expiry Date
- Oct 06, 2025
About this record
Access comprehensive regulatory information for "Remon" Proteus suspension staining reagent and Proteus agglutination serum (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b59f72073df2a65928b00f3984f5ca01 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.
Free DatabasePowered by Pure Global AI89,000+ Devices