Taiwan FDA registration 4dd79f5c0ed206d3447a3a97ffa0b97d
Singularity IgE External Parts Tube Fluid (Not Sterile)
TW: 英尤凱 特異性IgE外部品管液 (未滅菌)
Taiwan·Risk Class 1·PHADIA AB·Registered Mar 20, 2015 – Mar 20, 2030ActiveRegistration details
- Analysis ID
- 4dd79f5c0ed206d3447a3a97ffa0b97d
- Customs Code
- DHA09401501800
Company information
- Manufacturer
- PHADIA AB
- Manufacturer Country
- Sweden
- 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Mar 20, 2015
- Expiry Date
- Mar 20, 2030
About this record
Access comprehensive regulatory information for Singularity IgE External Parts Tube Fluid (Not Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4dd79f5c0ed206d3447a3a97ffa0b97d and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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