Taiwan FDA registration 6afaa5482dc896b67cbe4193ff309bfd
Ilia Fibrillarin antibody detection reagent
TW: 宜立亞Fibrillarin抗體檢測試劑
Taiwan·Risk Class 2·PHADIA AB;; PHADIA GMBH·Registered Jun 19, 2013 – Jun 19, 2028ActiveRegistration details
- Analysis ID
- 6afaa5482dc896b67cbe4193ff309bfd
- Customs Code
- DHA00602515105
Company information
- Manufacturer
- PHADIA AB;; PHADIA GMBH
- Manufacturer Country
- Sweden;;Germany
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- This product is used for the in vitro quantitative determination of Fibrillarin IgG antibodies in human serum and plasma on Phadia 100 and Phadia 250 instruments.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.5100 抗核抗體免疫試驗系統
- Import Information
- import
Dates and status
- Registration Date
- Jun 19, 2013
- Expiry Date
- Jun 19, 2028
About this record
Access comprehensive regulatory information for Ilia Fibrillarin antibody detection reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6afaa5482dc896b67cbe4193ff309bfd and manufactured by PHADIA AB;; PHADIA GMBH. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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