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“DIACOR” Patient Transport Stretcher (Non-Sterile) - Taiwan Registration e0d60518bf63be7ad6d32692293ac71e

Access comprehensive regulatory information for “DIACOR” Patient Transport 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 e0d60518bf63be7ad6d32692293ac71e and manufactured by DIACOR. The authorized representative in Taiwan is SSGI TAIWAN CO..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIACOR, and 1 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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e0d60518bf63be7ad6d32692293ac71e
Registration Details
Taiwan FDA Registration: e0d60518bf63be7ad6d32692293ac71e
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Device Details

“DIACOR” Patient Transport Stretcher (Non-Sterile)
TW: “戴蔻”病人運送推床 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

e0d60518bf63be7ad6d32692293ac71e

Ministry of Health Medical Device Import No. 014590

DHA09401459007

Company Information

United States

Product Details

J General hospital and personal use equipment

J6910 Wheeled stretcher

Imported from abroad

Dates and Status

Oct 21, 2014

Oct 21, 2019

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延

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