Taiwan FDA registration 4c9264c6e1be3ad030a8759f1f1b1d7a
INNOVANCE VWF Ac
TW: 伊諾凡司凡衛樂本試劑
Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Jul 10, 2020 – Jul 10, 2025ExpiredRegistration details
- Analysis ID
- 4c9264c6e1be3ad030a8759f1f1b1d7a
- License Form
- Ministry of Health Medical Device Import No. 033503
- Customs Code
- DHA05603350302
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Intended Use
- A test method for automatic detection of the activity of von Willebrand factor (VWF) in human citrate-containing plasma by particle enhancement.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- Factor B7290 deficiency test
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 10, 2020
- Expiry Date
- Jul 10, 2025
About this record
Access comprehensive regulatory information for INNOVANCE VWF Ac in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c9264c6e1be3ad030a8759f1f1b1d7a and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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