Taiwan FDA registration e124ae17f85e05a130d68b9bfc27c11d

“Wonderful” Alternating pressure air flotation mattress (Non-Sterile)

TW: “穩得福” 交替式壓力氣墊床 (未滅菌)

Taiwan·Risk Class 1·MD·SEQUOIA-TWN HEALTHCARE CO., LTD.·Registered Oct 29, 2020 – Oct 29, 2025Expired

Registration details

Analysis ID: e124ae17f85e05a130d68b9bfc27c11d
License Form: Ministry of Health Medical Device Manufacturing No. 008658

Company information

Manufacturer: SEQUOIA-TWN HEALTHCARE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FUGI ASSISTIVE DEVICE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5550 Alternating pressure air mattress
Import Information: Produced in Taiwan, China; Contract manufacturing

Dates and status

Registration Date: Oct 29, 2020
Expiry Date: Oct 29, 2025

About this record

Access comprehensive regulatory information for “Wonderful” Alternating pressure air flotation 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 e124ae17f85e05a130d68b9bfc27c11d and manufactured by SEQUOIA-TWN HEALTHCARE CO., LTD.. The authorized representative in Taiwan is FUGI ASSISTIVE DEVICE CO., LTD..

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