"Dayi" alternating pressure air mattress (unsterilized) - Taiwan Registration f627aa773ad3fbb30b43c4de993304fe
Access comprehensive regulatory information for "Dayi" alternating pressure air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f627aa773ad3fbb30b43c4de993304fe and manufactured by Dayi Medical Instrument Factory. The authorized representative in Taiwan is Dayi Medical Instrument 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.
Device Details
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
J.5550 ไบคๆฟๅผๅฃๅๆฐฃๅขๅบ
Domestic
Dates and Status
May 20, 2009
May 20, 2014
Dec 14, 2016
Cancellation Information
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