Pure Global

"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.

Free Database
Powered by Pure Global AI
89,000+ Devices
6a053eebcae2bcbcc48deff3eee790ea
Registration Details
Taiwan FDA Registration: 6a053eebcae2bcbcc48deff3eee790ea
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Stryker" Alternating pressure air flotation mattress (Non-Sterile)
TW: "ๅฒๆณฐๅ…‹"ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

6a053eebcae2bcbcc48deff3eee790ea

Ministry of Health Medical Device Import No. 015076

DHA09401507601

Company Information

United States

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

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€