Pure Global

Helena Electrophoresis Analyzer (Non-Sterile) - Taiwan Registration d93fbad127b435ceb352acb0f447fe4d

Access comprehensive regulatory information for Helena Electrophoresis Analyzer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d93fbad127b435ceb352acb0f447fe4d and manufactured by Helena Laboratories Corp.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..

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
d93fbad127b435ceb352acb0f447fe4d
Registration Details
Taiwan FDA Registration: d93fbad127b435ceb352acb0f447fe4d
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Helena Electrophoresis Analyzer (Non-Sterile)
TW: ๆตทๅ€ซ้‚ฃ้›ปๆณณๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d93fbad127b435ceb352acb0f447fe4d

Ministry of Health Medical Device Import Registration No. 003050

DHA08400305007

Company Information

United States

Product Details

Electrophoresis equipment used in clinical practice is a device that uses a specific buffer medium to separate molecules or particles, including plasma proteins, lipoproteins, enzymes and heme, according to a net charge. This device is often used with certain substances to measure various analytical substances to aid in the diagnosis and treatment of various diseases.

A Clinical chemistry and clinical toxicology

A2485 Electrophoresis equipment for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026