Taiwan FDA registration 54096213e704a5253e9326121188c9a8
ImmunoCAP Phadiatop Infant
TW: 英尤凱嬰幼兒過敏體質篩檢試劑
Taiwan·Risk Class 2·MD·PHADIA AB·Registered Mar 21, 2016 – Mar 21, 2026ExpiredRegistration details
- Analysis ID
- 54096213e704a5253e9326121188c9a8
- License Form
- Ministry of Health Medical Device Import No. 028302
- Customs Code
- DHA05602830208
Company information
- Manufacturer
- PHADIA AB
- Manufacturer Country
- Sweden
- Authorized Representative
- PHADIA TAIWAN INC.
Product details
- Intended Use
- Performance changes (new applicable models) are: as detailed in the approved version of the Chinese manual.
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5510 Immunoglobulins A, G, M, D and E Immunoassay System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 21, 2016
- Expiry Date
- Mar 21, 2026
About this record
Access comprehensive regulatory information for ImmunoCAP Phadiatop Infant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54096213e704a5253e9326121188c9a8 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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