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"Siemens" basic phosphate per (diethanolamine method) reagent set - Taiwan Registration 8206a557e315a845c7419f76c4e8c8dc

Access comprehensive regulatory information for "Siemens" basic phosphate per (diethanolamine method) reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8206a557e315a845c7419f76c4e8c8dc and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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8206a557e315a845c7419f76c4e8c8dc
Registration Details
Taiwan FDA Registration: 8206a557e315a845c7419f76c4e8c8dc
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Device Details

"Siemens" basic phosphate per (diethanolamine method) reagent set
TW: โ€œ่ฅฟ้–€ๅญโ€้นผๆ€ง็ฃท้…ธๆฏ (ไบŒไน™้†‡่ƒบๆณ•) ่ฉฆๅŠ‘็ต„
Risk Class 2

Registration Details

8206a557e315a845c7419f76c4e8c8dc

DHA00601998401

Company Information

Product Details

The activity of alkaline phosphate in human serum and plasma is quantitatively determined on the ADVIA automated chemical analysis system.

A Clinical chemistry and clinical toxicology

A.1050 Alkaline phosphatase or isoenzyme testing system

Contract manufacturing;; input

Dates and Status

Apr 09, 2009

Apr 09, 2024