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“Linet” EMERGENCY STRETCHER (Non-Sterile) - Taiwan Registration b6bef13b2e2860864b2909c23ddd7cbb

Access comprehensive regulatory information for “Linet” EMERGENCY 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 b6bef13b2e2860864b2909c23ddd7cbb and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is MEDICAL-MASTER 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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b6bef13b2e2860864b2909c23ddd7cbb
Registration Details
Taiwan FDA Registration: b6bef13b2e2860864b2909c23ddd7cbb
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Device Details

“Linet” EMERGENCY STRETCHER (Non-Sterile)
TW: “里內特” 急診推床 (未滅菌)
Risk Class 1
MD

Registration Details

b6bef13b2e2860864b2909c23ddd7cbb

Ministry of Health Medical Device Import No. 019264

DHA09401926406

Company Information

Czechia

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 04, 2018

Jul 04, 2023