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"Yao-Hong" stretcher (Non-Sterile) - Taiwan Registration 73cb7871555122cff3fc25e96d44fb9a

Access comprehensive regulatory information for "Yao-Hong" stretcher (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 73cb7871555122cff3fc25e96d44fb9a and manufactured by YAO HONG INSTRUMENT PLANT CO., LTD.. The authorized representative in Taiwan is YAO HONG INSTRUMENT PLANT 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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73cb7871555122cff3fc25e96d44fb9a
Registration Details
Taiwan FDA Registration: 73cb7871555122cff3fc25e96d44fb9a
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Device Details

"Yao-Hong" stretcher (Non-Sterile)
TW: "่€€ๅฎ" ๆ‰‹ๆๅผๆ“”ๆžถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

73cb7871555122cff3fc25e96d44fb9a

Ministry of Health Medical Device Manufacturing Registration No. 003130

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Portable Stretcher (J.6900)".

J General hospital and personal use equipment

J6900 portable stretcher

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025