Taiwan FDA registration 89442fa90feb62bef2764bd6f0eb9a8f
"Dybo" IMMUNOQUICK C. Difficile GDH (Non-Sterile)
TW: "帝博" 英諾魁困難梭狀桿菌快速檢測試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·BIOSYNEX·Registered Sep 11, 2015 – Sep 11, 2020CancelledRegistration details
- Analysis ID
- 89442fa90feb62bef2764bd6f0eb9a8f
- License Form
- Ministry of Health Medical Device Import No. 015658
- Customs Code
- DHA09401565807
Company information
- Manufacturer
- BIOSYNEX
- Manufacturer Country
- France
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 11, 2015
- Expiry Date
- Sep 11, 2020
- Cancellation Date
- May 06, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Dybo" IMMUNOQUICK C. Difficile GDH (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 89442fa90feb62bef2764bd6f0eb9a8f and manufactured by BIOSYNEX. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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