Taiwan FDA registration 9ee0a31bb682c836083ea6be70cef75f

"SIGMA-CARE" Alternation Pressure-Relief System (Non-Sterile)

TW: "亞護"交替防褥瘡氣墊床組(未滅菌)

Taiwan·Risk Class 1·MD·The second plant of Yahu Development Co., Ltd·Registered Feb 21, 2020 – Feb 21, 2025Expired

Registration details

Analysis ID: 9ee0a31bb682c836083ea6be70cef75f
License Form: Ministry of Health Medical Device Manufacturing No. 008204

Company information

Manufacturer: The second plant of Yahu Development Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: The second plant of Yahu Development 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

Dates and status

Registration Date: Feb 21, 2020
Expiry Date: Feb 21, 2025

About this record

Access comprehensive regulatory information for "SIGMA-CARE" Alternation Pressure-Relief System (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 9ee0a31bb682c836083ea6be70cef75f and manufactured by The second plant of Yahu Development Co., Ltd. The authorized representative in Taiwan is The second plant of Yahu Development Co., Ltd.

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