"Stryker" Alternating pressure air flotation mattress (Non-Sterile) - Taiwan Registration 6a053eebcae2bcbcc48deff3eee790ea
Access comprehensive regulatory information for "Stryker" 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 6a053eebcae2bcbcc48deff3eee790ea and manufactured by STRYKER MEDICAL. The authorized representative in Taiwan is Meide Medical Devices 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.
Device Details
Registration Details
6a053eebcae2bcbcc48deff3eee790ea
Ministry of Health Medical Device Import No. 015076
DHA09401507601
Product Details
J General hospital and personal use equipment
J5550 Alternating pressure air mattress
Imported from abroad
Dates and Status
Apr 07, 2015
Apr 07, 2020
Aug 05, 2022
Cancellation Information
Logged out
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