Taiwan FDA registration 833f1eebb22dd5092e90832ed9393e16
Espert fully automated enterovirus real-time detection PCR kit
TW: 艾斯柏特全自動腸病毒即時偵測PCR套組
Registration details
- Analysis ID
- 833f1eebb22dd5092e90832ed9393e16
- Customs Code
- DHA00601961203
Company information
- Manufacturer
- CEPHEID
- Manufacturer Country
- United States
- Authorized Representative
- PROGRESSIVE GROUP INC.
Product details
- Intended Use
- The RT-PCR principle was used to detect enterovirus RNA in cerebrospinal fluid in patients with symptoms and symptoms of meningitis.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.0001 腸病毒71型血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 12, 2008
- Expiry Date
- Dec 12, 2028
About this record
Access comprehensive regulatory information for Espert fully automated enterovirus real-time detection PCR kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 833f1eebb22dd5092e90832ed9393e16 and manufactured by CEPHEID. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
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