Taiwan FDA registration d92bba0b36cc16cbf50e930b313f7972
Fukushima Quick-take Streptococcus B Rapid Assay Reagent
TW: 福島快取鏈球菌B群快速測定試劑
Taiwan·Risk Class 1·VEDA LAB·Registered Dec 22, 2005 – Dec 22, 2010CancelledRegistration details
- Analysis ID
- d92bba0b36cc16cbf50e930b313f7972
- Customs Code
- DHA04400230308
Company information
- Manufacturer
- VEDA LAB
- Manufacturer Country
- France
- Authorized Representative
- Fukushima Medical Equipment Co., Ltd
Product details
- Intended Use
- Qualitative detection of group B streptococcal antigen in human vaginal specimens.
- 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
- Dec 22, 2005
- Expiry Date
- Dec 22, 2010
- Cancellation Date
- Nov 20, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Fukushima Quick-take Streptococcus B Rapid Assay Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d92bba0b36cc16cbf50e930b313f7972 and manufactured by VEDA LAB. The authorized representative in Taiwan is Fukushima Medical Equipment Co., Ltd.
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