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"Helena" QuickGel Lactate Dehydrogenase Reagent kit (Non-sterile) - Taiwan Registration efa589240037898364b9a2ac050ef656

Access comprehensive regulatory information for "Helena" QuickGel Lactate Dehydrogenase Reagent kit (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 efa589240037898364b9a2ac050ef656 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, INC., 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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efa589240037898364b9a2ac050ef656
Registration Details
Taiwan FDA Registration: efa589240037898364b9a2ac050ef656
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Device Details

"Helena" QuickGel Lactate Dehydrogenase Reagent kit (Non-sterile)
TW: "่ณ€่“ฎ้‚ฃ" ไนณ้…ธ่„ซๆฐซ้…ถ่ฉฆๅŠ‘็ต„ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

efa589240037898364b9a2ac050ef656

Ministry of Health Medical Device Import No. 018623

DHA09401862303

Company Information

United States

Product Details

Limited to the first level recognition range of lactate dehydrogenase test system (A.1440) of the management method for medical devices.

A Clinical chemistry and clinical toxicology

A1440 Lactate dehydrogenase test system

Imported from abroad

Dates and Status

Dec 19, 2017

Dec 19, 2022

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