Pure Global

"Siemens" San Dino zinc reagent - Taiwan Registration f9b5accb6d941853c821da108df57b4a

Access comprehensive regulatory information for "Siemens" San Dino zinc reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f9b5accb6d941853c821da108df57b4a and manufactured by SENTINEL CH. SPA. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
f9b5accb6d941853c821da108df57b4a
Registration Details
Taiwan FDA Registration: f9b5accb6d941853c821da108df57b4a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" San Dino zinc reagent
TW: "่ฅฟ้–€ๅญ" ่–ๅธ่ซพ ้‹…่ฉฆๅŠ‘
Risk Class 2

Registration Details

f9b5accb6d941853c821da108df57b4a

DHA05603586007

Company Information

Italy

Product Details

This product is used in vitro diagnostics to determine zinc concentration in serum and plasma using direct colorimetry (without protein removal) in combination with Atellica CH Analyzer.

A Clinical chemistry and clinical toxicology

A.9999 Miscellaneous ;; A.1150 calibration

Input;; QMS/QSD

Dates and Status

Sep 30, 2022

Sep 30, 2027