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"Helena" electrophoresis analyzer (unsterilized) - Taiwan Registration 598a4542205bcd0d52bcb797d528e62c

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 598a4542205bcd0d52bcb797d528e62c 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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598a4542205bcd0d52bcb797d528e62c
Registration Details
Taiwan FDA Registration: 598a4542205bcd0d52bcb797d528e62c
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Device Details

"Helena" electrophoresis analyzer (unsterilized)
TW: "ๆตทๅ€ซ้‚ฃ" ้›ปๆณณๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

598a4542205bcd0d52bcb797d528e62c

DHA04401039601

Company Information

United States

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

Logged out

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