Taiwan FDA registration d963a874a1c5402d0056f7afd0548767
"Quick Test" Fetal Curvature Teratogenus Rapid Test Reagent (Unsterilized)
TW: "速測" 胎兒彎曲畸形菌屬快速檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Dec 29, 2011 – Dec 29, 2016CancelledRegistration details
- Analysis ID
- d963a874a1c5402d0056f7afd0548767
- Customs Code
- DHA04401124702
Company information
- Manufacturer
- CERTEST BIOTEC S.L.
- Manufacturer Country
- Spain
- Authorized Representative
- JOLEX INTERNATIONAL CO., LTD.
Product details
- Intended Use
- It is limited to the first level of identification of the medical device management measures "Curved malformation foetus serum reagent (C.3110)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3110 胎兒彎曲桿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2011
- Expiry Date
- Dec 29, 2016
- Cancellation Date
- Mar 06, 2017
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Quick Test" Fetal Curvature Teratogenus Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d963a874a1c5402d0056f7afd0548767 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..
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