Taiwan FDA registration 439b196c4069ba5acab018483caacf15

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 Aug 28, 2020 – Aug 28, 2025Cancelled
Registration details
Analysis ID
439b196c4069ba5acab018483caacf15
License Form
Ministry of Health Medical Device Import No. 021906
Customs Code
DHA09402190602
Company information
Manufacturer Country
United States
Authorized Representative
DAYCARE HEALTH CO., LTD.
Product details
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
Aug 28, 2020
Expiry Date
Aug 28, 2025
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 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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