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“PE&LE ENTERPRISE” Alternating pressure air flotation mattress (Non-sterile) - Taiwan Registration da06767e1a2d9a7a8cc04a9ece3bf78a

Access comprehensive regulatory information for “PE&LE ENTERPRISE” 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 da06767e1a2d9a7a8cc04a9ece3bf78a and manufactured by PE & LE ENTERPRISE LTD.. The authorized representative in Taiwan is PE & LE ENTERPRISE LTD..

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da06767e1a2d9a7a8cc04a9ece3bf78a
Registration Details
Taiwan FDA Registration: da06767e1a2d9a7a8cc04a9ece3bf78a
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Device Details

“PE&LE ENTERPRISE” Alternating pressure air flotation mattress (Non-sterile)
TW: “派立” 交替式壓力氣墊床(未滅菌)
Risk Class 1
MD

Registration Details

da06767e1a2d9a7a8cc04a9ece3bf78a

Ministry of Health Medical Device Manufacturing No. 007825

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".

J General hospital and personal use equipment

J5550 Alternating pressure air mattress

Produced in Taiwan, China

Dates and Status

Jun 28, 2019

Jun 28, 2024