Pure Global

Sanmeng urea liquid test system - Taiwan Registration dab724ab20e8d39fc26fa810f074e5c7

Access comprehensive regulatory information for Sanmeng urea liquid test system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dab724ab20e8d39fc26fa810f074e5c7 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..

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
dab724ab20e8d39fc26fa810f074e5c7
Registration Details
Taiwan FDA Registration: dab724ab20e8d39fc26fa810f074e5c7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Sanmeng urea liquid test system
TW: ไธ‰็›Ÿ ๅฐฟ็ด ๆถฒ้ซ”่ฉฆ้ฉ—็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

dab724ab20e8d39fc26fa810f074e5c7

DHA00602075002

Product Details

It is used to quantify urea in human serum, blood or urine in vitro

A Clinical chemistry and clinical toxicology

A.1770 ๅฐฟ็ด ๆฐฎ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Dec 18, 2009

Dec 18, 2014

Apr 25, 2018

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ