Taiwan FDA registration ec3d59e35d4ee07d76efa94fc0919d67

“LUMARK” Truncal Orthosis (Non-Sterile)

TW: “璐瑪”軀幹裝具(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Luma Enterprises Limited New House Factory·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
ec3d59e35d4ee07d76efa94fc0919d67
License Form
Ministry of Health Medical Device Manufacturing Registration No. 008096
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LU MARK ENTERPRISES INC.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3490 Torso Gear
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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