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DAYCARE Truncal orthosis (Non-Sterile) - Taiwan Registration 439b196c4069ba5acab018483caacf15

Access comprehensive regulatory information for DAYCARE Truncal orthosis (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 439b196c4069ba5acab018483caacf15 and manufactured by MINNESOTA RESUSCITATION SOLUTIONS, D.B.D ADVANCEDCPR SOLUTION. The authorized representative in Taiwan is DAYCARE HEALTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MINNESOTA RESUSCITATION SOLUTIONS, D.B.D ADVANCEDCPR SOLUTION, 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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439b196c4069ba5acab018483caacf15
Registration Details
Taiwan FDA Registration: 439b196c4069ba5acab018483caacf15
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Device Details

DAYCARE Truncal orthosis (Non-Sterile)
TW: ่‰พ็›Š่พฐ ่ป€ๅนน่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

439b196c4069ba5acab018483caacf15

Ministry of Health Medical Device Import No. 021906

DHA09402190602

Company Information

Product Details

o Equipment for physical medicine

O3490 Torso Gear

Imported from abroad

Dates and Status

Aug 28, 2020

Aug 28, 2025

Cancellation Information

Logged out

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