Taiwan FDA registration 7128dfd9d3082bdde767fcfeeecfa7f9
"Vertical spin" Clostridium difficile latex agglutination reagent (unsterilized)
TW: "立飛旋"困難梭菌乳膠凝集試劑(未滅菌)
Registration details
- Analysis ID
- 7128dfd9d3082bdde767fcfeeecfa7f9
- Customs Code
- DHA04401014104
Company information
- Manufacturer
- LIOFILCHEM S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2660 微生物鑑別及測定器材
- 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 "Vertical spin" Clostridium difficile 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 7128dfd9d3082bdde767fcfeeecfa7f9 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