Taiwan FDA registration aade5ab8a3c45d10da72c80e7f5328ca
"Ruimeng" Wakeella Streptococcus pneumoniae test kit (unsterilized)
TW: "銳盟" 威克菌肺炎鏈球菌檢測套組（未滅菌）
Taiwan·Risk Class 1·REMEL EUROPE LIMITED·Registered Oct 04, 2005 – Oct 04, 2025ExpiredRegistration details
- Analysis ID
- aade5ab8a3c45d10da72c80e7f5328ca
- Customs Code
- DHA04400075902
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- Qualitative detection of Streptococcus pneumoniae in body fluids and blood cultures.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3740 鏈球菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 04, 2005
- Expiry Date
- Oct 04, 2025
About this record
Access comprehensive regulatory information for "Ruimeng" Wakeella Streptococcus pneumoniae 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 aade5ab8a3c45d10da72c80e7f5328ca and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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