Taiwan FDA registration c7a033c58cdd23e51fdd97e8ed86fa5b

Liquichek Hematology Control (X)

TW: 立可測血液學品管液(X)

Taiwan·Risk Class 2·MD·BIO-RAD LABORATORIES·Registered Aug 26, 2013 – Aug 26, 2028Active

Registration details

Analysis ID: c7a033c58cdd23e51fdd97e8ed86fa5b
License Form: Ministry of Health Medical Device Import No. 025271
Customs Code: DHA05602527108

Company information

Manufacturer: BIO-RAD LABORATORIES
Manufacturer Country: United States
Authorized Representative: Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)

Product details

Intended Use: This product is a three-concentration tube solution designed to monitor the values obtained by the Sysmex Blood Analyzer.
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B8625 Hematological Quality Management Mixture
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 26, 2013
Expiry Date: Aug 26, 2028

About this record

Access comprehensive regulatory information for Liquichek Hematology Control (X) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c7a033c58cdd23e51fdd97e8ed86fa5b and manufactured by BIO-RAD LABORATORIES. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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