Taiwan FDA registration 4c484a44f7a7f0ef41b5411380d72082
Berecoron undifferentiated heparin low-concentration tube solution
TW: 倍瑞可隆未分化肝素低濃度品管液
Registration details
- Analysis ID
- 4c484a44f7a7f0ef41b5411380d72082
- Customs Code
- DHA00602378602
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- SYSMEX TAIWAN CO., LTD.
Product details
- Intended Use
- Use low concentration tubes for the quantification of undifferentiated heparin. Must be used in conjunction with the Belikoron heparin reagent.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.5425 Versatile system for in vitro agglutination studies
- Import Information
- import
Dates and status
- Registration Date
- Jul 03, 2012
- Expiry Date
- Jul 03, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Berecoron undifferentiated heparin low-concentration tube solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c484a44f7a7f0ef41b5411380d72082 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..
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