"K.F."Medical Mattress(Non-Sterile) - Taiwan Registration a662357e9b4f71088546f999df8ae305
Access comprehensive regulatory information for "K.F."Medical Mattress(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 a662357e9b4f71088546f999df8ae305 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.
Device Details
Registration Details
a662357e9b4f71088546f999df8ae305
Ministry of Health Medical Device Manufacturing Registration No. 000493
DHY08300049309
Product Details
It has the function of supporting the patient to prevent excessive pressure on the body part, and can be used to treat or avoid bedsores caused by bed rest.
J General hospital and personal use equipment
J5150 Non-powered treatment mattress
Produced in Taiwan, China
Dates and Status
Oct 01, 2021
Oct 31, 2025