Taiwan FDA registration d93fbad127b435ceb352acb0f447fe4d
Helena Electrophoresis Analyzer (Non-Sterile)
TW: 海倫那電泳分析儀(未滅菌)
Taiwan·Risk Class 1·MD·Helena Laboratories Corp.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- d93fbad127b435ceb352acb0f447fe4d
- License Form
- Ministry of Health Medical Device Import Registration No. 003050
- Customs Code
- DHA08400305007
Company information
- Manufacturer
- Helena Laboratories Corp.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2485 Electrophoresis equipment for clinical use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
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 DatabasePowered by Pure Global AI89,000+ Devices