Taiwan FDA registration 0e6d8b31c345aec5f670cb2c0d4f9b3e
Diagnostec Helicobacter Pylori Antigen Rapid Test Kit (Non-Sterile)
TW: 德克幽門螺旋桿菌檢測試劑盒 (未滅菌)
Taiwan·Risk Class 1·MD·Jei Daniel(JD) Biotech Corp.·Registered Jan 12, 2015 – Jan 12, 2020CancelledRegistration details
- Analysis ID
- 0e6d8b31c345aec5f670cb2c0d4f9b3e
- License Form
- Ministry of Health Medical Device Land Transport No. 002307
- Customs Code
- DHA09600230702
Company information
- Manufacturer
- Jei Daniel(JD) Biotech Corp.
- Manufacturer Country
- China
- Authorized Representative
- REININGHUN DIAGNOSTICS BIOMEDICAL CORPORATION
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C0003 Helicobacter serological reagent
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Jan 12, 2015
- Expiry Date
- Jan 12, 2020
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
About this record
Access comprehensive regulatory information for Diagnostec Helicobacter Pylori Antigen Rapid Test Kit (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 0e6d8b31c345aec5f670cb2c0d4f9b3e and manufactured by Jei Daniel(JD) Biotech Corp.. The authorized representative in Taiwan is REININGHUN DIAGNOSTICS BIOMEDICAL CORPORATION.
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