Taiwan FDA registration 2f8bcaf2e4d7191272b038b490dfc1d6
"Humasis" Influenza A/B Antigen Test (non-sterile)
TW: "優美適" 流感A/B型抗原檢測試劑組 (未滅菌)
Registration details
- Analysis ID
- 2f8bcaf2e4d7191272b038b490dfc1d6
- License Form
- Ministry of Health Medical Device Import No. 013869
- Customs Code
- DHA09401386900
Company information
- Manufacturer
- HUMASIS CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- LINKSEAS TRADING CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 24, 2014
- Expiry Date
- Feb 24, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Humasis" Influenza A/B Antigen Test (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2f8bcaf2e4d7191272b038b490dfc1d6 and manufactured by HUMASIS 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