Taiwan FDA registration a9e2d22f8e144b1460569817623dcdf1

"Beckman Coulter" analysis of specific reagents (unsterilized)

TW: "貝克曼庫爾特" 分析特定試劑(未滅菌)

Taiwan·Risk Class 1·IMMUNOTECH SAS, A BECKMAN COULTER COMPANY·Registered Apr 19, 2012 – Apr 19, 2017Cancelled

Registration details

Analysis ID: a9e2d22f8e144b1460569817623dcdf1
Customs Code: DHA04401161209

Company information

Manufacturer: IMMUNOTECH SAS, A BECKMAN COULTER COMPANY
Manufacturer Country: France
Authorized Representative: UNISYS BIOMEDICAL CO.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Analysis of Specific Reagents (B.4020)".
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.4020 Analysis of specific tests
Import Information: import

Dates and status

Registration Date: Apr 19, 2012
Expiry Date: Apr 19, 2017
Cancellation Date: Nov 04, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Beckman Coulter" analysis of specific reagents (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a9e2d22f8e144b1460569817623dcdf1 and manufactured by IMMUNOTECH SAS, A BECKMAN COULTER COMPANY. The authorized representative in Taiwan is UNISYS BIOMEDICAL CO..

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