Taiwan FDA registration 9005847b9df5bb70ca83c15956b997e4
"E-TAKE" EBV Test Kit (Non-Sterile)
TW: "醫達" EB病毒檢驗試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·MD BIOTECH CORPORATION·Registered Jan 29, 2014 – Jan 29, 2019CancelledRegistration details
- Analysis ID
- 9005847b9df5bb70ca83c15956b997e4
- License Form
- Ministry of Health Medical Device Import No. 013824
- Customs Code
- DHA09401382401
Company information
- Manufacturer
- MD BIOTECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- E-TAKE TECHNOLOGY CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3235 Epstein-Barr virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 29, 2014
- Expiry Date
- Jan 29, 2019
- Cancellation Date
- Aug 02, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "E-TAKE" EBV 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 9005847b9df5bb70ca83c15956b997e4 and manufactured by MD BIOTECH CORPORATION. The authorized representative in Taiwan is E-TAKE TECHNOLOGY CO., LTD..
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