Pure Global

"Uyishi" manual patient transport device - Taiwan Registration f493f9ec9c85e0f61053213569560b1a

Access comprehensive regulatory information for "Uyishi" manual patient transport device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f493f9ec9c85e0f61053213569560b1a and manufactured by WYEAST MEDICAL CORPORATION. The authorized representative in Taiwan is Tianqun Medical Enterprise 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
f493f9ec9c85e0f61053213569560b1a
Registration Details
Taiwan FDA Registration: f493f9ec9c85e0f61053213569560b1a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Uyishi" manual patient transport device
TW: โ€œ็ถญ้†ซไธ–โ€ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ
Risk Class 1
Cancelled

Registration Details

f493f9ec9c85e0f61053213569560b1a

DHA04400656802

Company Information

United States

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J.6785 Manual Patient Conveying Device

import

Dates and Status

Mar 11, 2008

Mar 11, 2013

Apr 24, 2015

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ