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“Artilat”Nonpowered flotation therapy mattress (Non-Sterile) - Taiwan Registration 1f168ba253e1c5bd4f485e107e3e1310

Access comprehensive regulatory information for “Artilat”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 1f168ba253e1c5bd4f485e107e3e1310 and manufactured by ARTILAT NV. The authorized representative in Taiwan is EVERCARE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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1f168ba253e1c5bd4f485e107e3e1310
Registration Details
Taiwan FDA Registration: 1f168ba253e1c5bd4f485e107e3e1310
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Device Details

“Artilat”Nonpowered flotation therapy mattress (Non-Sterile)
TW: “愛迪麗特”非動力式治療床墊(未滅菌)
Risk Class 1
MD

Registration Details

1f168ba253e1c5bd4f485e107e3e1310

Ministry of Health Medical Device Import Registration No. 012811

DHA08401281104

Company Information

Belgium

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".

J General hospital and personal use equipment

J5150 Non-powered treatment mattress

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023