Taiwan FDA registration 8e505fa9e85b206d943ab6b0744d9d02

"Lain Hong" Anti-decubitus Mattress (Non-Sterile)

TW: "聯鴻" 防褥瘡型床墊 (未滅菌)

Taiwan·Risk Class 1·MD·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Jan 25, 2022 – Oct 31, 2023Expired

Registration details

Analysis ID: 8e505fa9e85b206d943ab6b0744d9d02
License Form: Ministry of Health Medical Device Manufacturing Registration No. a00060

Company information

Manufacturer: SHIAN JIA MEEI ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: LAIN HONG SHING YEH CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "Non-powered Treatment Mattress (J.5150)" of the Classification and Grading Management Measures for Medical Equipment.
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: Jan 25, 2022
Expiry Date: Oct 31, 2023

About this record

Access comprehensive regulatory information for "Lain Hong" Anti-decubitus 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 8e505fa9e85b206d943ab6b0744d9d02 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is LAIN HONG SHING YEH CO., LTD..

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