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"Feno" portable stretcher (unsterilized) - Taiwan Registration 88bb099b179adb204c3839b643159f5e

Access comprehensive regulatory information for "Feno" portable stretcher (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88bb099b179adb204c3839b643159f5e 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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88bb099b179adb204c3839b643159f5e
Registration Details
Taiwan FDA Registration: 88bb099b179adb204c3839b643159f5e
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Device Details

"Feno" portable stretcher (unsterilized)
TW: "่ฒป่ซพ" ๆ‰‹ๆๅผๆ“”ๆžถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

88bb099b179adb204c3839b643159f5e

DHA04401007007

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.6900 Hand-held stretcher

import

Dates and Status

Mar 21, 2011

Mar 21, 2026

Sep 30, 2021

Cancellation Information

Logged out

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