Taiwan FDA registration 5ef8f46c6a1db2dc5656bc69451d4be8

"Helena" Touch Electrophoresis Analyzer (Unsterilized)

TW: "海倫那" 觸控式電泳分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HELENA LABORATORIES CORP·Registered Dec 20, 2016 – Dec 20, 2026Cancelled
Registration details
Analysis ID
5ef8f46c6a1db2dc5656bc69451d4be8
Customs Code
DHA09401731207
Company information
Manufacturer Country
United States
Authorized Representative
SHANG LI INSTRUMENTS CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of "Electrophoresis Equipment for Clinical Use (A.2485)" under the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2485 Electrophoresis equipment for clinical use
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Dec 20, 2016
Expiry Date
Dec 20, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Helena" Touch 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 5ef8f46c6a1db2dc5656bc69451d4be8 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.

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