Taiwan FDA registration ff9323cf52625454df083d0f1c74c81c

"SK MEDITECH" Nonpowered flotation therapy mattress (non-sterile)

TW: "舒況麥迪泰克" 非動力式治療床墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SK MEDITECH. CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
ff9323cf52625454df083d0f1c74c81c
License Form
Ministry of Health Medical Device Import Registration No. 022235
Customs Code
DHA08402223500
Company information
Manufacturer Country
Korea, Republic of
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J5150 Non-powered treatment mattress
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

Access comprehensive regulatory information for "SK MEDITECH" Nonpowered flotation therapy mattress (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 ff9323cf52625454df083d0f1c74c81c and manufactured by SK MEDITECH. CO., LTD.. The authorized representative in Taiwan is Shiang Tai Medical Instructment CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SK MEDITECH. CO., LTD., 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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