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“Trulife” Truncal orthosis (Non-Sterile) - Taiwan Registration f1f1606413c1f0310e8172a7b8d2bc6e

Access comprehensive regulatory information for “Trulife” 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 f1f1606413c1f0310e8172a7b8d2bc6e and manufactured by TRULIFE INC. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRULIFE 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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f1f1606413c1f0310e8172a7b8d2bc6e
Registration Details
Taiwan FDA Registration: f1f1606413c1f0310e8172a7b8d2bc6e
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Device Details

“Trulife” Truncal orthosis (Non-Sterile)
TW: “儲來福” 軀幹裝具 (未滅菌)
Risk Class 1
MD

Registration Details

f1f1606413c1f0310e8172a7b8d2bc6e

Ministry of Health Medical Device Import Registration No. 016118

DHA08401611800

Company Information

United States

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

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

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