"Helena" capillary electrophoresis analyzer (unsterilized) - Taiwan Registration ec2fc620b9a1a6d619f3fe0f1d382e0d
Access comprehensive regulatory information for "Helena" capillary 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 ec2fc620b9a1a6d619f3fe0f1d382e0d 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, 1 companies making similar products including HELENA LABORATORIES CORP., and 1 recent registrations in the same category. 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.
Device Details
Product Details
Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
A Clinical chemistry and clinical toxicology
A.2485 Electrophoresis equipment for clinical use
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
May 25, 2011
May 25, 2026
Sep 30, 2021
Cancellation Information
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