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“LUMARK” Truncal Orthosis (Non-Sterile) - Taiwan Registration ec3d59e35d4ee07d76efa94fc0919d67

Access comprehensive regulatory information for “LUMARK” Truncal Orthosis (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 ec3d59e35d4ee07d76efa94fc0919d67 and manufactured by Luma Enterprises Limited New House Factory. The authorized representative in Taiwan is LU MARK ENTERPRISES INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Luma Enterprises Limited New House Factory, 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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ec3d59e35d4ee07d76efa94fc0919d67
Registration Details
Taiwan FDA Registration: ec3d59e35d4ee07d76efa94fc0919d67
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Device Details

“LUMARK” Truncal Orthosis (Non-Sterile)
TW: “璐瑪”軀幹裝具(未滅菌)
Risk Class 1
MD

Registration Details

ec3d59e35d4ee07d76efa94fc0919d67

Ministry of Health Medical Device Manufacturing Registration No. 008096

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".

o Equipment for physical medicine

O3490 Torso Gear

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025

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