Taiwan FDA registration 85cf30b2adb299a48016b629a8c441ec
HEMOCHRON Whole Blood Microcoagulation Analyzer
TW: 漢莫克微量凝血時間測定儀
Taiwan·Risk Class 2·MD·Accriva Diagnostics Inc.·Registered Jul 24, 2013 – Jul 24, 2028ActiveRegistration details
- Analysis ID
- 85cf30b2adb299a48016b629a8c441ec
- License Form
- Ministry of Health Medical Device Import No. 025093
- Customs Code
- DHA05602509300
Company information
- Manufacturer
- Accriva Diagnostics Inc.
- Manufacturer Country
- United States
- Authorized Representative
- Werfen Taiwan Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Jul 24, 2013
- Expiry Date
- Jul 24, 2028
About this record
Access comprehensive regulatory information for HEMOCHRON Whole Blood Microcoagulation Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 85cf30b2adb299a48016b629a8c441ec and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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