Taiwan FDA registration 3cf71002bb471d88b9cad3eb4db85708

Berecoron undifferentiated heparin high-concentration tube solution

TW: 倍瑞可隆未分化肝素高濃度品管液

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Registered Jul 03, 2012 – Jul 03, 2022Cancelled

Registration details

Analysis ID: 3cf71002bb471d88b9cad3eb4db85708
Customs Code: DHA00602367006

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
Manufacturer Country: Germany
Authorized Representative: SYSMEX TAIWAN CO., LTD.

Product details

Intended Use: Use high concentration tube solutions for quantitative analysis 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 high-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 3cf71002bb471d88b9cad3eb4db85708 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SYSMEX TAIWAN CO., LTD..

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