Taiwan FDA registration a185a258fb9931d1ee021f0c912cde5d
"GPN" Helicobacter pylori reagent ( Non-Sterile)
TW: "芯世代"幽門螺旋桿菌試劑(未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Mar 05, 2015 – Mar 05, 2020CancelledRegistration details
- Analysis ID
- a185a258fb9931d1ee021f0c912cde5d
- License Form
- Ministry of Health Medical Device Import No. 014967
- Customs Code
- DHA09401496702
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)
- C0003 Helicobacter serological 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" Helicobacter pylori 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 a185a258fb9931d1ee021f0c912cde5d and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is GENPRONEX INC..
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