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"Orliman" Limb orthosis (Non-Sterile) - Taiwan Registration 149afb05bfbed48cb061a48ce4b04f2e

Access comprehensive regulatory information for "Orliman" Limb 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 149afb05bfbed48cb061a48ce4b04f2e and manufactured by ORLIMAN. The authorized representative in Taiwan is LIESIEN ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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149afb05bfbed48cb061a48ce4b04f2e
Registration Details
Taiwan FDA Registration: 149afb05bfbed48cb061a48ce4b04f2e
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Device Details

"Orliman" Limb orthosis (Non-Sterile)
TW: "ๆญ็ซ‹็›Ÿ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

149afb05bfbed48cb061a48ce4b04f2e

Ministry of Health Medical Device Import No. 016080

DHA09401608007

Company Information

Spain

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Jan 15, 2016

Jan 15, 2021

Aug 04, 2023

Cancellation Information

Logged out

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