Taiwan FDA registration 98f89c313777a94cccb00c82933e8c61
"Lipixuan" streptococcal latex agglutination reagent (unsterilized)
TW: "立飛旋"鏈球菌乳膠凝集試劑(未滅菌)
Taiwan·Risk Class 1·LIOFILCHEM S.R.L.·Registered Apr 06, 2011 – Apr 06, 2016CancelledRegistration details
- Analysis ID
- 98f89c313777a94cccb00c82933e8c61
- Customs Code
- DHA04401013904
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Restriction of medical device management methods Streptococcus belongs to the first level identification range of serum reagent (C.3740).
- 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
- Apr 06, 2011
- Expiry Date
- Apr 06, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Lipixuan" streptococcal latex agglutination reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98f89c313777a94cccb00c82933e8c61 and manufactured by LIOFILCHEM S.R.L.. The authorized representative in Taiwan is DYBO ENTERPRISE 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