Taiwan FDA registration a662357e9b4f71088546f999df8ae305

"K.F."Medical Mattress(Non-Sterile)

TW: "國發"醫用床墊(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: a662357e9b4f71088546f999df8ae305
License Form: Ministry of Health Medical Device Manufacturing Registration No. 000493
Customs Code: DHY08300049309

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: 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.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5150 Non-powered treatment mattress
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."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..

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