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"HELY AND WEBER" Limb orthosis (Non-Sterile) - Taiwan Registration 705d2e6839e192b164410ade08878870

Access comprehensive regulatory information for "HELY AND WEBER" 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 705d2e6839e192b164410ade08878870 and manufactured by HELY AND WEBER. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELY AND WEBER, 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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705d2e6839e192b164410ade08878870
Registration Details
Taiwan FDA Registration: 705d2e6839e192b164410ade08878870
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Device Details

"HELY AND WEBER" Limb orthosis (Non-Sterile)
TW: "่ตซ่މๅ‰ไผฏ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

705d2e6839e192b164410ade08878870

Ministry of Health Medical Device Import Registration No. 020112

DHA08402011200

Company Information

United States

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

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2024

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