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"FERNO" NAJO Backboard(Non-Sterile) - Taiwan Registration 3092f4e712cfc21af208caaa11fd3b41

Access comprehensive regulatory information for "FERNO" NAJO Backboard(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 3092f4e712cfc21af208caaa11fd3b41 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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3092f4e712cfc21af208caaa11fd3b41
Registration Details
Taiwan FDA Registration: 3092f4e712cfc21af208caaa11fd3b41
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Device Details

"FERNO" NAJO Backboard(Non-Sterile)
TW: "่ฒป่ซพ"้•ท่ƒŒๆฟ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

3092f4e712cfc21af208caaa11fd3b41

Ministry of Health Medical Device Import Registration No. 010068

DHA08401006804

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".

J General hospital and personal use equipment

J6900 portable stretcher

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026