Taiwan FDA registration f113387cf7ecef2d10d45866244031ae

"Chaiduo Weixin" analysis of specific reagents (unsterilized)

TW: "柴多微訊" 分析特定試劑 (未滅菌)

Taiwan·Risk Class 1·ZYTOVISION GMBH·Registered Nov 18, 2011 – Nov 18, 2016Cancelled

Registration details

Analysis ID: f113387cf7ecef2d10d45866244031ae
Customs Code: DHA04401106700

Company information

Manufacturer: ZYTOVISION GMBH
Manufacturer Country: Germany
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: Nov 18, 2011
Expiry Date: Nov 18, 2016
Cancellation Date: May 17, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Chaiduo Weixin" 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 f113387cf7ecef2d10d45866244031ae and manufactured by ZYTOVISION GMBH. The authorized representative in Taiwan is UNISYS BIOMEDICAL CO..

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