Taiwan FDA registration 075b13ebb250573b10e46b19787a1f0b

DAYCARE Truncal orthosis (Non-Sterile)

TW: 艾益辰 軀幹裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MINNESOTA RESUSCITATION SOLUTIONS, D.B.D ADVANCEDCPR SOLUTION·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
075b13ebb250573b10e46b19787a1f0b
License Form
Ministry of Health Medical Device Import Registration No. 021906
Customs Code
DHA08402190603
Company information
Manufacturer Country
United States
Authorized Representative
DAYCARE HEALTH CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3490 Torso Gear
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

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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