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“LUMARK” Truncal Orthosis (Non-Sterile) - Taiwan Registration 4a0c8693533659538b176f41ecd04d5f

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 4a0c8693533659538b176f41ecd04d5f 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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4a0c8693533659538b176f41ecd04d5f
Registration Details
Taiwan FDA Registration: 4a0c8693533659538b176f41ecd04d5f
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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
Cancelled

Registration Details

4a0c8693533659538b176f41ecd04d5f

Ministry of Health Medical Device Manufacturing No. 008096

Company Information

Taiwan, Province of China

Product Details

o Equipment for physical medicine

O3490 Torso Gear

Produced in Taiwan, China

Dates and Status

Dec 23, 2019

Dec 23, 2024

Cancellation Information

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