Taiwan FDA registration b7c78b67294cc12d641a4de06bf08cd2

Mitsubishi automatic latex immunoassay system

TW: 三菱全自動乳膠免疫分析系統
Taiwan flagTaiwan·Risk Class 1·MITSUBISHI CHEMICAL MEDIENCE CORPORATION YACHIYO AREA·Registered Nov 11, 2005 – Nov 11, 2015Cancelled
Registration details
Analysis ID
b7c78b67294cc12d641a4de06bf08cd2
Customs Code
DHA04400188502
Company information
Manufacturer Country
Japan
Authorized Representative
Jingxiang Co., Ltd
Product details
Intended Use
Serum and plasma were taken as analysis samples, and tumor markers, immunoglobulins, drug concentrations, and serum proteins were measured by latex agglutination near-infrared turbidimetry (LPIA), immunoturbidimetry (TIA), and colorimetry.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.5700 Human whole plasma or serum immunoassay system
Import Information
import
Dates and status
Registration Date
Nov 11, 2005
Expiry Date
Nov 11, 2015
Cancellation Date
Jun 07, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Mitsubishi automatic latex immunoassay system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b7c78b67294cc12d641a4de06bf08cd2 and manufactured by MITSUBISHI CHEMICAL MEDIENCE CORPORATION YACHIYO AREA. The authorized representative in Taiwan is Jingxiang Co., Ltd.

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