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“FERNO” BACKBOARD STRETCHER (Non-Sterile) - Taiwan Registration 91abb4719fcd0180bc28a2ba9733ac92

Access comprehensive regulatory information for “FERNO” BACKBOARD 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 91abb4719fcd0180bc28a2ba9733ac92 and manufactured by FERNO-WASHINGTON, INC.. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FERNO-WASHINGTON, INC., and 3 recent registrations in the same category. 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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91abb4719fcd0180bc28a2ba9733ac92
Registration Details
Taiwan FDA Registration: 91abb4719fcd0180bc28a2ba9733ac92
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Device Details

“FERNO” BACKBOARD STRETCHER (Non-Sterile)
TW: “婓諾” 長背板擔架 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

91abb4719fcd0180bc28a2ba9733ac92

Ministry of Health Medical Device Import No. 015780

DHA09401578004

Company Information

United States

Product Details

J General hospital and personal use equipment

J6900 portable stretcher

Imported from abroad

Dates and Status

Oct 26, 2015

Oct 26, 2025

Cancellation Information

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