Taiwan FDA registration b33307a12caf5c0819dd0959bcbf2871
"GPN" Influenza virus reagent (Non-sterile)
TW: "芯世代"流行性感冒病毒試劑(未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Mar 05, 2015 – Mar 05, 2020CancelledRegistration details
- Analysis ID
- b33307a12caf5c0819dd0959bcbf2871
- License Form
- Ministry of Health Medical Device Import No. 014966
- Customs Code
- DHA09401496600
Company information
- Manufacturer
- MD BIOTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- GENPRONEX INC.
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
- Mar 05, 2015
- Expiry Date
- Mar 05, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "GPN" Influenza virus reagent (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 b33307a12caf5c0819dd0959bcbf2871 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is GENPRONEX INC..
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