Taiwan FDA registration a83bbd869c7dc8436716314811719fb6
"Vircell" VARICELLA-ZOSTER ELISA IgG/IgM
TW: "凡爾賽"水痘帶狀皰疹病毒酵素免疫分析法IgG/IgM試劑組
Taiwan·Risk Class 2·MD·VIRCELL, S.L·Registered Mar 17, 2020 – Mar 17, 2025ExpiredRegistration details
- Analysis ID
- a83bbd869c7dc8436716314811719fb6
- License Form
- Ministry of Health Medical Device Import No. 033294
- Customs Code
- DHA05603329403
Company information
- Manufacturer
- VIRCELL, S.L
- Manufacturer Country
- Spain
- Authorized Representative
- Abbott Rapid Diagnostics Health Corp.
Product details
- Intended Use
- This product uses indirect immunoenzyme analysis to detect IgG and/or IgM antibodies against varicella zoster virus in human serum/plasma.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3900 Varicella zoster virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 17, 2020
- Expiry Date
- Mar 17, 2025
About this record
Access comprehensive regulatory information for "Vircell" VARICELLA-ZOSTER ELISA IgG/IgM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a83bbd869c7dc8436716314811719fb6 and manufactured by VIRCELL, S.L. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..
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