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“SmartEm” BACKBOARD STRETCHER (Non-Sterile) - Taiwan Registration 83d8bc58df4cea0359e0ade88e3e3fce

Access comprehensive regulatory information for “SmartEm” BACKBOARD 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 83d8bc58df4cea0359e0ade88e3e3fce and manufactured by SmartEm GmbH. The authorized representative in Taiwan is SALVO ENTERPRISE CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SmartEm GmbH, 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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83d8bc58df4cea0359e0ade88e3e3fce
Registration Details
Taiwan FDA Registration: 83d8bc58df4cea0359e0ade88e3e3fce
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Device Details

“SmartEm” BACKBOARD STRETCHER (Non-Sterile)
TW: “斯馬特恩”長背板擔架(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

83d8bc58df4cea0359e0ade88e3e3fce

Ministry of Health Medical Device Import No. 022482

DHA09402248200

Company Information

Germany

Product Details

J General hospital and personal use equipment

J6900 portable stretcher

Imported from abroad

Dates and Status

Apr 15, 2021

Apr 15, 2026

Cancellation Information

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