Taiwan FDA registration 2a0925b9880be2349fe3d9d98f627dbd

Shinohara uric acid correction solution

TW: 筱原尿酸校正液

Taiwan·Risk Class 2·SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER·Registered Jul 13, 2022 – Jul 13, 2027Active

Registration details

Analysis ID: 2a0925b9880be2349fe3d9d98f627dbd
Customs Code: DHA05603567703

Company information

Manufacturer: SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER
Manufacturer Country: Japan
Authorized Representative: MEDICARE PRODUCTS INC.

Product details

Intended Use: This product is a calibration solution used by an automatic analyzer to measure uric acid concentration.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1150 Calibrated Products
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jul 13, 2022
Expiry Date: Jul 13, 2027

About this record

Access comprehensive regulatory information for Shinohara uric acid correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2a0925b9880be2349fe3d9d98f627dbd and manufactured by SHINO-TEST CORPORATION, SAGAMIHARA PRODUCTION CENTER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

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