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"FERNO" Stretcher (Non-Sterile)  - Taiwan Registration 6e9c18c4b7ec6c3cc315888199fc30d2

Access comprehensive regulatory information for "FERNO" 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 6e9c18c4b7ec6c3cc315888199fc30d2 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is ADEPT GENERAL CORP..

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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6e9c18c4b7ec6c3cc315888199fc30d2
Registration Details
Taiwan FDA Registration: 6e9c18c4b7ec6c3cc315888199fc30d2
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Device Details

"FERNO" Stretcher (Non-Sterile) 
TW: "費諾" 手提式擔架 (未滅菌)
Risk Class 1
MD

Registration Details

6e9c18c4b7ec6c3cc315888199fc30d2

Ministry of Health Medical Device Import Registration No. 010070

DHA08401007004

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

J6900 portable stretcher

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026