"HELY AND WEBER" Limb orthosis (Non-Sterile)
- Analysis ID
- 705d2e6839e192b164410ade08878870
- License Form
- Ministry of Health Medical Device Import Registration No. 020112
- Customs Code
- DHA08402011200
- Manufacturer
- HELY AND WEBER
- Manufacturer Country
- United States
- Authorized Representative
- ORTHOHEALTH CO., LTD.
- 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
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
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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.