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“DIACOR” Patient Transport Stretcher (Non-Sterile) - Taiwan Registration 15f9009ec257e68c82efdbb76bbf8a6a

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 15f9009ec257e68c82efdbb76bbf8a6a 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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15f9009ec257e68c82efdbb76bbf8a6a
Registration Details
Taiwan FDA Registration: 15f9009ec257e68c82efdbb76bbf8a6a
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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

Registration Details

15f9009ec257e68c82efdbb76bbf8a6a

Ministry of Health Medical Device Import No. 021715

DHA09402171505

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Wheeled Stretcher (J.6910)".

J General hospital and personal use equipment

J6910 Wheeled stretcher

Imported from abroad

Dates and Status

Jul 08, 2020

Jul 08, 2025

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