Taiwan FDA registration 9eca01c2d7f88527c0ed433da32fbeb8
"Dybo" IMMUNOQUICK TOX A/B (Non-Sterile)
TW: "帝博" 英諾魁困難梭狀芽孢桿菌A/B毒素快速檢測試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·BIOSYNEX·Registered Oct 05, 2015 – Oct 05, 2020CancelledRegistration details
- Analysis ID
- 9eca01c2d7f88527c0ed433da32fbeb8
- License Form
- Ministry of Health Medical Device Import No. 015716
- Customs Code
- DHA09401571608
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
- Oct 05, 2015
- Expiry Date
- Oct 05, 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 TOX A/B (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 9eca01c2d7f88527c0ed433da32fbeb8 and manufactured by BIOSYNEX. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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