Taiwan FDA registration e7988601d83ce49bf5e0fd0315ef2cd1
Abbott ICE Syphilis
TW: 亞培梅毒螺旋體試劑組
Taiwan·Risk Class 2·MD·DIASORIN S.P.A. UK BRANCH·Registered May 25, 2018 – May 25, 2023CancelledRegistration details
- Analysis ID
- e7988601d83ce49bf5e0fd0315ef2cd1
- License Form
- Ministry of Health Medical Device Import No. 031119
- Customs Code
- DHA05603111901
Company information
- Manufacturer
- DIASORIN S.P.A. UK BRANCH
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3830 Treponema pallidum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 25, 2018
- Expiry Date
- May 25, 2023
- Cancellation Date
- May 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Abbott ICE Syphilis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e7988601d83ce49bf5e0fd0315ef2cd1 and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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