Taiwan FDA registration 529f6d17cfe69d67bdc8adf5357fe402
ILIA AUTOIMMUNE EXTERNAL QUALITY CONTROL SOLUTION (UNSTERILIZED)
TW: 宜立亞 自體免疫外部品管液 (未滅菌)
Taiwan·Risk Class 1·PHADIA AB;; PHADIA GMBH·Registered Apr 07, 2015 – Apr 07, 2025ExpiredRegistration details
- Analysis ID
- 529f6d17cfe69d67bdc8adf5357fe402
- Customs Code
- DHA09401507904
Company information
- Manufacturer
- PHADIA AB;; PHADIA GMBH
- Manufacturer Country
- Sweden;;Germany
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Apr 07, 2015
- Expiry Date
- Apr 07, 2025
About this record
Access comprehensive regulatory information for ILIA AUTOIMMUNE EXTERNAL QUALITY CONTROL SOLUTION (UNSTERILIZED) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 529f6d17cfe69d67bdc8adf5357fe402 and manufactured by PHADIA AB;; PHADIA GMBH. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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