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“Sterisets” Alternating Pressure Air Flotation Mattress (Non-Sterile) - Taiwan Registration c449df75d2ade28139417371af3e180c

Access comprehensive regulatory information for “Sterisets” 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 c449df75d2ade28139417371af3e180c and manufactured by STERISETS MEDICAL PRODUCTS. The authorized representative in Taiwan is CHAMP MEDICS CO., LTD..

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.

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c449df75d2ade28139417371af3e180c
Registration Details
Taiwan FDA Registration: c449df75d2ade28139417371af3e180c
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Device Details

“Sterisets” Alternating Pressure Air Flotation Mattress (Non-Sterile)
TW: “史瑞得” 交替式壓力氣墊床 (未滅菌)
Risk Class 1
MD

Registration Details

c449df75d2ade28139417371af3e180c

Ministry of Health Medical Device Import No. 021876

DHA09402187603

Company Information

Portugal

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

Imported from abroad

Dates and Status

Aug 20, 2020

Aug 20, 2025