Taiwan FDA registration 83d8bf74a3bebd20fd2210a954ff25d2
"Remeng" Wicker * Neisseria meningococcus B / E. coli K1 test kit
TW: 〝銳盟〞威克菌*奈瑟氏腦膜炎球菌 B 群/大腸桿菌K1型檢測套組
Taiwan·Risk Class 2·REMEL EUROPE LIMITED·Registered Dec 07, 2005 – Dec 07, 2015CancelledRegistration details
- Analysis ID
- 83d8bf74a3bebd20fd2210a954ff25d2
- Customs Code
- DHA00601530908
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SCN TRADING COMPANY LIMITED
Product details
- Intended Use
- A rapid latex assay for the qualitative detection of antigens of Neisseri's meningitis (meningococcal) group B and E. coli K1 in body fluids or blood culture supernatants as a result of infection.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3390 奈瑟氏菌屬直接血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 07, 2005
- Expiry Date
- Dec 07, 2015
- Cancellation Date
- May 17, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Remeng" Wicker * Neisseria meningococcus B / E. coli K1 test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 83d8bf74a3bebd20fd2210a954ff25d2 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.
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