Taiwan FDA registration 1a7c9d96ad9610e096763660ce14a7bb

Sameng Alkaline Phosphoric Acid (Unitary Each) Test System (2 parts liquid)

TW: 三盟 鹼性磷酸(酉每)試驗系統(2部分液體)
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER·Registered Dec 16, 2009 – Dec 16, 2014Cancelled
Registration details
Analysis ID
1a7c9d96ad9610e096763660ce14a7bb
Customs Code
DHA00602074203
Company information
Manufacturer Country
United States
Authorized Representative
MEDICARE PRODUCTS INC.
Product details
Intended Use
It is used to quantify the alkaline phosphoric acid in human serum or plasma in vitro in a manual or automated system
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1050 Alkaline phosphatase or isoenzyme testing system
Import Information
import
Dates and status
Registration Date
Dec 16, 2009
Expiry Date
Dec 16, 2014
Cancellation Date
Apr 25, 2018
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for Sameng Alkaline Phosphoric Acid (Unitary Each) Test System (2 parts liquid) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a7c9d96ad9610e096763660ce14a7bb and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

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