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Taiwan FDA registration 32e0aeb37185abbabde467c532d6486e

Shinohara uric acid test reagent

TW: 筱原尿酸檢驗試劑
Taiwan flagTaiwan·Risk Class 1·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Oct 06, 2010 – Oct 06, 2015Cancelled
Registration details
Analysis ID
32e0aeb37185abbabde467c532d6486e
Customs Code
DHA04400931307
Company information
Manufacturer
SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER
Manufacturer Country
Japan
Authorized Representative
BEAM INTERNATIONAL INC.
Product details
Intended Use
Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1775 尿酸試驗系統
Import Information
import
Dates and status
Registration Date
Oct 06, 2010
Expiry Date
Oct 06, 2015
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 Shinohara uric acid test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32e0aeb37185abbabde467c532d6486e and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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