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"Gufeng" non-powered treatment mattress (unsterilized) - Taiwan Registration 0620c798ec7dba7e4e03976b3552833f

Access comprehensive regulatory information for "Gufeng" 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 0620c798ec7dba7e4e03976b3552833f and manufactured by Gufeng Instrument Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is TYMED INSTRUMENTS COMPANY.

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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0620c798ec7dba7e4e03976b3552833f
Registration Details
Taiwan FDA Registration: 0620c798ec7dba7e4e03976b3552833f
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Device Details

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

Registration Details

0620c798ec7dba7e4e03976b3552833f

Company Information

Taiwan, Province of China

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

Domestic

Dates and Status

May 05, 2009

May 05, 2014

Dec 14, 2016

Cancellation Information

Logged out

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