Taiwan FDA registration 9341dd4ae92fac6583e9bc523e7c979e
"HURN ARNG" Truncal Orthosis (Non-Sterile)
TW: "宏昂" 軀幹裝具 (未滅菌)
Registration details
- Analysis ID
- 9341dd4ae92fac6583e9bc523e7c979e
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 005210
Company information
- Manufacturer
- HURN ARNG ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HURN ARNG ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3490 Torso Gear
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for "HURN ARNG" Truncal 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 9341dd4ae92fac6583e9bc523e7c979e and manufactured by HURN ARNG ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HURN ARNG 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.
Free DatabasePowered by Pure Global AI89,000+ Devices