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Daejeon plastic portable stretcher (unsterilized) - Taiwan Registration 0d66d6cc51042531f551da0f20d1abac

Access comprehensive regulatory information for Daejeon plastic 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 0d66d6cc51042531f551da0f20d1abac and manufactured by AMERICA BUSINESS OF CALIFONIA. The authorized representative in Taiwan is EZ-CARE INSTRUMENTS. 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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0d66d6cc51042531f551da0f20d1abac
Registration Details
Taiwan FDA Registration: 0d66d6cc51042531f551da0f20d1abac
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Device Details

Daejeon plastic portable stretcher (unsterilized)
TW: ๅคง็”ฐ็‰Œๅก‘่† ๆ‰‹ๆๅผๆ“”ๆžถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

0d66d6cc51042531f551da0f20d1abac

DHA04400157306

Company Information

United States

Product Details

The portable stretcher is made of high-density polyethylene integrally molded, which is suitable for carrying patients with accidental injuries, injuries or fainting.

J General hospital and personal use equipment

J.6900 Hand-held stretcher

import

Dates and Status

Oct 30, 2005

Oct 30, 2020

Aug 05, 2022

Cancellation Information

Logged out

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