Taiwan FDA registration 52d6eb636fa58833fa067231bbf6f958

"JP" Alternating pressure air flotation mattress (Non-Sterile)

TW: "建鵬" 交替式壓力氣墊床 (未滅菌)

Taiwan·Risk Class 1·MD·Noble Industrial Co., Ltd. Chiayi Factory·Registered Feb 03, 2017 – Feb 03, 2027Active

Registration details

Analysis ID: 52d6eb636fa58833fa067231bbf6f958
License Form: Ministry of Health Medical Device Manufacturing No. 006585

Company information

Manufacturer: Noble Industrial Co., Ltd. Chiayi Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Noble Industrial Co., Ltd. Chiayi Factory

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 03, 2017
Expiry Date: Feb 03, 2027

About this record

Access comprehensive regulatory information for "JP" 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 52d6eb636fa58833fa067231bbf6f958 and manufactured by Noble Industrial Co., Ltd. Chiayi Factory. The authorized representative in Taiwan is Noble Industrial Co., Ltd. Chiayi Factory.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.