Taiwan FDA registration b28a95bc77f5888b1810061a2d158468
"CerTest" Adenovirus Respiratory (Non-Sterile)
TW: "速測" 腺病毒(呼吸道)快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·CERTEST BIOTEC, S.L.·Registered Dec 22, 2016 – Dec 22, 2021CancelledRegistration details
- Analysis ID
- b28a95bc77f5888b1810061a2d158468
- License Form
- Ministry of Health Medical Device Import No. 017328
- Customs Code
- DHA09401732809
Company information
- Manufacturer
- CERTEST BIOTEC, S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3020 adenovirus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2016
- Expiry Date
- Dec 22, 2021
- Cancellation Date
- Mar 09, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "CerTest" Adenovirus Respiratory (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 b28a95bc77f5888b1810061a2d158468 and manufactured by CERTEST BIOTEC, S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL 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