Taiwan FDA registration 2318664fec369bdedb2a54c4dacfdcd9
ILIA IGG Corrective Reagent Group
TW: 宜立亞IgG校正試劑組
Taiwan·Risk Class 2·PHADIA AB·Registered Mar 26, 2015 – Mar 26, 2030ActiveRegistration details
- Analysis ID
- 2318664fec369bdedb2a54c4dacfdcd9
- Customs Code
- DHA05602719005
Company information
- Manufacturer
- PHADIA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- Performance changes (added applicable models): This product needs to be equipped with Fadia 100, Fadia 200 and Fadia 250 instruments, Ilia IgG correction solution/ILIA IgG correction sheet needs to use the microwell groove of the ILIA IgG correction to establish the IgG correction curve to analyze the patient specimen, and the ILIA IgG correction curve quality control fluid/the quality of the ILIA IgG correction curve quality control sheet needs to use the microwell groove for the use of the ILIA IgG correction curve to control the effectiveness of the IgG correction curve.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- import
Dates and status
- Registration Date
- Mar 26, 2015
- Expiry Date
- Mar 26, 2030
About this record
Access comprehensive regulatory information for ILIA IGG Corrective Reagent Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2318664fec369bdedb2a54c4dacfdcd9 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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