Taiwan FDA registration b05838209ea33d90b57aef1c46ca4c3a
Helena electrophoresis analyzer (unsterilized)
TW: 海倫那電泳分析儀(未滅菌)
Registration details
- Analysis ID
- b05838209ea33d90b57aef1c46ca4c3a
- Customs Code
- DHA04400305000
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)
- A.2485 Electrophoresis equipment for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Mar 21, 2006
- Expiry Date
- Mar 21, 2026
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Helena electrophoresis analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b05838209ea33d90b57aef1c46ca4c3a 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