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New Non-Powered Floating Treatment Mattress (Non-Sterilized) - Taiwan Registration e5587db8293ff9f70bf732cac792f79b

Access comprehensive regulatory information for New Non-Powered Floating Treatment Mattress (Non-Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e5587db8293ff9f70bf732cac792f79b and manufactured by Singa Technology Co., Ltd. Chiayi Factory. The authorized representative in Taiwan is Singa Technology Co., Ltd. Chiayi Factory.

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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e5587db8293ff9f70bf732cac792f79b
Registration Details
Taiwan FDA Registration: e5587db8293ff9f70bf732cac792f79b
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Device Details

New Non-Powered Floating Treatment Mattress (Non-Sterilized)
TW: ๆ–ฐๅŠ  ้žๅ‹•ๅŠ›ๅผๆตฎๅ‹•ๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

e5587db8293ff9f70bf732cac792f79b

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the "Non-powered Floating Treatment Mattress (J.5150)" of the Measures for the Classification and Grading of Medical Devices.

J General hospital and personal use equipment

J.5150 Non-powered floating therapy mattress

Domestic

Dates and Status

May 08, 2024

Oct 31, 2025