Taiwan FDA registration f423803b385fc21acf3e320482101110

"K.F." ARM SLING(NON-STERILE)

TW: "國發" 手臂吊帶(未滅菌)

Taiwan·Risk Class 1·MD·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired

Registration details

Analysis ID: f423803b385fc21acf3e320482101110
License Form: Ministry of Health Medical Device Manufacturing Registration No. 000041
Customs Code: DHY08300004100

Company information

Manufacturer: K.F. MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K.F. MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: The arm is secured by a cloth strap that hangs around the neck.
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3640 arm sling
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2025

About this record

Access comprehensive regulatory information for "K.F." ARM SLING(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 f423803b385fc21acf3e320482101110 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS 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.