Taiwan FDA registration 019ac0e5b513f2fda5db81b8c5ad3bbf
Reagent for the detection of IgG affinity of Toxoplasma relyshanensis
TW: 禮亞尚弓漿蟲IgG親和性檢測試劑
Taiwan·Risk Class 2·DIASORIN S.P.A.·Registered Jan 11, 2013 – Jan 11, 2018CancelledRegistration details
- Analysis ID
- 019ac0e5b513f2fda5db81b8c5ad3bbf
- Customs Code
- DHA00602431402
Company information
- Manufacturer
- DIASORIN S.P.A.
- Manufacturer Country
- Italy
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- This product uses chemical cold light immunoassay technology (CLIA) to detect the affinity of IgG antibodies to Toxoplasmagondii in human serum and plasma.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3780 弓漿蟲血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Jan 11, 2013
- Expiry Date
- Jan 11, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Reagent for the detection of IgG affinity of Toxoplasma relyshanensis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 019ac0e5b513f2fda5db81b8c5ad3bbf and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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