Taiwan FDA registration e7d6616d4d1cb7425ace77af88f51a5c
"Bioresearch" Shigella antiserum microbial reagent
TW: "生研" 志賀氏菌抗血清微生物試劑
Registration details
- Analysis ID
- e7d6616d4d1cb7425ace77af88f51a5c
- Customs Code
- DHA04400521003
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Hong Kong Commercial Mérieux S.p.A. Taiwan Branch
Product details
- Intended Use
- Limited to the first level identification range of Shigella serological reagents (C.3660) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3660 志賀氏桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Oct 02, 2006
- Expiry Date
- Oct 02, 2011
- Cancellation Date
- Nov 27, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bioresearch" Shigella antiserum microbial reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e7d6616d4d1cb7425ace77af88f51a5c and manufactured by DENKA SEIKEN CO., LTD.. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.
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