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
Taiwan flagTaiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Jul 03, 2012 – Jul 03, 2022Cancelled
Registration details
Analysis ID
4c484a44f7a7f0ef41b5411380d72082
Customs Code
DHA00602378602
Company information
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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