Pure Global

"Siemens" immunoglobulin G analysis reagent - Taiwan Registration 60c7f445234d8b585c10e2170362255c

Access comprehensive regulatory information for "Siemens" immunoglobulin G analysis reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60c7f445234d8b585c10e2170362255c and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. 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
60c7f445234d8b585c10e2170362255c
Registration Details
Taiwan FDA Registration: 60c7f445234d8b585c10e2170362255c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Siemens" immunoglobulin G analysis reagent
TW: โ€œ่ฅฟ้–€ๅญโ€ ๅ…็–ซ็ƒ่›‹็™ฝGๅˆ†ๆž่ฉฆๅŠ‘
Risk Class 2

Registration Details

60c7f445234d8b585c10e2170362255c

DHA05603177203

Company Information

Product Details

This product is used in vitro diagnostics with Atellica CH Analyzer to quantitatively detect immunoglobulin G (IgG) in human serum and plasma (heparin lithium).

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Nov 02, 2018

Nov 02, 2028