Taiwan FDA registration 60cab16ddadf914b7cba7cda62aea96a
"Bioken" streptococcus is a pneumococcal antiserum
TW: 「生研」鏈球菌屬肺炎雙球菌抗血清
Registration details
- Analysis ID
- 60cab16ddadf914b7cba7cda62aea96a
- Customs Code
- DHA04400434600
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- LINKSEAS TRADING CO., LTD.
Product details
- 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
- May 04, 2006
- Expiry Date
- May 04, 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 "Bioken" streptococcus is a pneumococcal antiserum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 60cab16ddadf914b7cba7cda62aea96a and manufactured by DENKA SEIKEN CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING 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