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"Astek" Limb Protector (Non-Sterile) - Taiwan Registration 211fb0242f6708aa04013e3c8dadfc17

Access comprehensive regulatory information for "Astek" Limb Protector (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 211fb0242f6708aa04013e3c8dadfc17 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY 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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211fb0242f6708aa04013e3c8dadfc17
Registration Details
Taiwan FDA Registration: 211fb0242f6708aa04013e3c8dadfc17
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Device Details

"Astek" Limb Protector (Non-Sterile)
TW: "ไบžๆ˜Ÿ" ่‚ข้ซ”่ญทๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

211fb0242f6708aa04013e3c8dadfc17

Ministry of Health Medical Device Manufacturing Registration No. 005770

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025