Taiwan FDA registration 705d2e6839e192b164410ade08878870

"HELY AND WEBER" Limb orthosis (Non-Sterile)

TW: "赫莉偉伯" 肢體裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HELY AND WEBER·Registered Oct 01, 2021 – Oct 31, 2024Expired
Registration details
Analysis ID
705d2e6839e192b164410ade08878870
License Form
Ministry of Health Medical Device Import Registration No. 020112
Customs Code
DHA08402011200
Company information
Manufacturer
HELY AND WEBER
Manufacturer Country
United States
Authorized Representative
ORTHOHEALTH CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3475 Body Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2024
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About this record

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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