Taiwan FDA registration 36c807fa3e2b8b963162937f315081ba

"Urotek" Truncal orthosis (Non-Sterile)

TW: 婕新軀幹裝具(未滅菌)

Taiwan·Risk Class 1·MD·NANTONG JINGFANG HUI TEXTILE TECHNOLOGY CO., LTD·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 36c807fa3e2b8b963162937f315081ba
License Form: Ministry of Health Medical Device Land Transport Registration No. 004426
Customs Code: DHA08600442608

Company information

Manufacturer: NANTONG JINGFANG HUI TEXTILE TECHNOLOGY CO., LTD
Manufacturer Country: China
Authorized Representative: DOUBLE NET INTERNATIONAL 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: Imported from abroad; Made in China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for "Urotek" 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 36c807fa3e2b8b963162937f315081ba and manufactured by NANTONG JINGFANG HUI TEXTILE TECHNOLOGY CO., LTD. The authorized representative in Taiwan is DOUBLE NET INTERNATIONAL 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.