Taiwan FDA registration bdeddb5fae8a9a04a4abd12fa2a46926
"MIZUHO" INFLUENZA A/B RAPID TEST (Non-Sterile)
TW: "美日和" 流感A/B型快速檢測試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·MIZUHO MEDY CO., LTD.·Registered Nov 16, 2015 – Nov 16, 2020CancelledRegistration details
- Analysis ID
- bdeddb5fae8a9a04a4abd12fa2a46926
- License Form
- Ministry of Health Medical Device Import No. 015864
- Customs Code
- DHA09401586400
Company information
- Manufacturer
- MIZUHO MEDY CO., LTD.
- Manufacturer Country
- Japan
- 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
- Nov 16, 2015
- Expiry Date
- Nov 16, 2020
- 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 "MIZUHO" INFLUENZA A/B RAPID 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 bdeddb5fae8a9a04a4abd12fa2a46926 and manufactured by MIZUHO MEDY CO., LTD.. The authorized representative in Taiwan is LINKSEAS TRADING CO., LTD..
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