Taiwan FDA registration 6c18f5291a10036465cdcb84de03376e
"Abbott" Alinity i 2nd Generation Testosterone Reagent Kit (Non-Sterile)
TW: "亞培"第二代睪丸脂酮試劑組(未滅菌)
Taiwan·Risk Class 1·MD·Axis-Shield Diagnostics Limited·Registered Mar 05, 2018 – Mar 05, 2028ActiveRegistration details
- Analysis ID
- 6c18f5291a10036465cdcb84de03376e
- License Form
- Ministry of Health Medical Device Import No. 018860
- Customs Code
- DHA09401886004
Company information
- Manufacturer
- Axis-Shield Diagnostics Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Limited to the first level identification range of the "testicular lipoketone test system (A.1680)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1680 Testicular Lipoketone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 05, 2018
- Expiry Date
- Mar 05, 2028
About this record
Access comprehensive regulatory information for "Abbott" Alinity i 2nd Generation Testosterone Reagent Kit (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6c18f5291a10036465cdcb84de03376e and manufactured by Axis-Shield Diagnostics Limited. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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