Taiwan FDA registration f200d4f60dad6ce54a984263bf501776

"MEDEPOT" Alternating Pressure Air Flotation Mattress (Non-Sterile)

TW: "美迪寶" 交替式壓力氣墊床 (未滅菌)

Taiwan·Risk Class 1·MD·Changyi Precision Industry Co., Ltd. precision factory·Registered Jan 24, 2018 – Jan 24, 2023Expired

Registration details

Analysis ID: f200d4f60dad6ce54a984263bf501776
License Form: Ministry of Health Medical Device Manufacturing No. 007093

Company information

Manufacturer: Changyi Precision Industry Co., Ltd. precision factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: MEDEPOT 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: Jan 24, 2018
Expiry Date: Jan 24, 2023

About this record

Access comprehensive regulatory information for "MEDEPOT" 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 f200d4f60dad6ce54a984263bf501776 and manufactured by Changyi Precision Industry Co., Ltd. precision factory. The authorized representative in Taiwan is MEDEPOT CO., LTD.

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