Taiwan FDA registration 7fd35d6105cf2b2a356ef7cfd3aa0d0e
IL ACL Elite Pro
TW: 實驗儀器公司全自動凝血分析儀
Taiwan·Risk Class 2·MD·INSTRUMENTATION LABORATORY CO.·Registered Aug 04, 2017 – Aug 04, 2027ActiveRegistration details
- Analysis ID
- 7fd35d6105cf2b2a356ef7cfd3aa0d0e
- License Form
- Ministry of Health Medical Device Import No. 029816
- Customs Code
- DHA05602981605
Company information
- Manufacturer
- INSTRUMENTATION LABORATORY CO.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- This product is an automatic analysis system for blood coagulation test and fibrinolysis test.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B5425 Multifunctional equipment for in vitro agglutination research
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2017
- Expiry Date
- Aug 04, 2027
About this record
Access comprehensive regulatory information for IL ACL Elite Pro in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7fd35d6105cf2b2a356ef7cfd3aa0d0e and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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