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DAYCARE Truncal orthosis (Non-Sterile) - Taiwan Registration 075b13ebb250573b10e46b19787a1f0b

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 075b13ebb250573b10e46b19787a1f0b 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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075b13ebb250573b10e46b19787a1f0b
Registration Details
Taiwan FDA Registration: 075b13ebb250573b10e46b19787a1f0b
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Device Details

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

Registration Details

075b13ebb250573b10e46b19787a1f0b

Ministry of Health Medical Device Import Registration No. 021906

DHA08402190603

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".

o Equipment for physical medicine

O3490 Torso Gear

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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