Taiwan FDA registration d1edf9312d953e93adf597929db901cc
"GPN" Mycobacterium tuberculosis immuno reagent (Non-Sterile)
TW: "芯世代"結核桿菌免疫試劑(未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Mar 05, 2015 – Mar 05, 2020CancelledRegistration details
- Analysis ID
- d1edf9312d953e93adf597929db901cc
- License Form
- Ministry of Health Medical Device Import No. 014965
- Customs Code
- DHA09401496501
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)
- C3370 Mycobacterium tuberculosis immunofluorescent 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" Mycobacterium tuberculosis immuno 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 d1edf9312d953e93adf597929db901cc and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is GENPRONEX INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices