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"Yilong" non-powered treatment mattress (unsterilized) - Taiwan Registration 918a34b7f86c6b4f14e888f25635ac33

Access comprehensive regulatory information for "Yilong" non-powered treatment mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 918a34b7f86c6b4f14e888f25635ac33 and manufactured by HILL-ROM MANUFACTURING, INC.. The authorized representative in Taiwan is CONPLUS INTERNATIONAL 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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918a34b7f86c6b4f14e888f25635ac33
Registration Details
Taiwan FDA Registration: 918a34b7f86c6b4f14e888f25635ac33
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Device Details

"Yilong" non-powered treatment mattress (unsterilized)
TW: โ€œๅฑน้พโ€้žๅ‹•ๅŠ›ๅผๆฒป็™‚ๅบŠๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

918a34b7f86c6b4f14e888f25635ac33

DHA04400783300

Company Information

United States

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

J.5150 Non-powered floating therapy mattress

import

Dates and Status

Jun 17, 2009

Jun 17, 2024

Sep 30, 2021

Cancellation Information

Logged out

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