Taiwan FDA registration 2554c02a6ef70fdcce43b80298fab003
"GPN" Listeria (Non-Sterile)
TW: "芯世代"李斯特菌快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Mar 09, 2015 – Mar 09, 2020CancelledRegistration details
- Analysis ID
- 2554c02a6ef70fdcce43b80298fab003
- License Form
- Ministry of Health Medical Device Import No. 014979
- Customs Code
- DHA09401497909
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)
- C3355 Listeria serological reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 09, 2015
- Expiry Date
- Mar 09, 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" Listeria (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 2554c02a6ef70fdcce43b80298fab003 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is GENPRONEX INC..
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