Taiwan FDA registration e94f443f2f23a3c5ecb928e45606991d
"Coris" Legionella K set (Non-Sterile)
TW: "科里斯" 退伍軍人菌體套組 (未滅菌)
Taiwan·Risk Class 1·MD·CORIS BIOCONCEPT·Registered Apr 20, 2015 – Apr 20, 2020CancelledRegistration details
- Analysis ID
- e94f443f2f23a3c5ecb928e45606991d
- License Form
- Ministry of Health Medical Device Import No. 015129
- Customs Code
- DHA09401512906
Company information
- Manufacturer
- CORIS BIOCONCEPT
- Manufacturer Country
- Belgium
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3300 Haemophilus serology
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2015
- Expiry Date
- Apr 20, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證逾有效期未申請展延
About this record
Access comprehensive regulatory information for "Coris" Legionella K set (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 e94f443f2f23a3c5ecb928e45606991d and manufactured by CORIS BIOCONCEPT. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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