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SENTEQ Flotation cushion (non-sterile) - Taiwan Registration f8d40b480e826d9b74143862b64565a4

Access comprehensive regulatory information for SENTEQ Flotation cushion (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 f8d40b480e826d9b74143862b64565a4 and manufactured by SENTEQ CO., LTD.. The authorized representative in Taiwan is SENTEQ 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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f8d40b480e826d9b74143862b64565a4
Registration Details
Taiwan FDA Registration: f8d40b480e826d9b74143862b64565a4
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Device Details

SENTEQ Flotation cushion (non-sterile)
TW: ็™ปๅบท็พŽ ๆตฎๅ‹•ๅๅขŠ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f8d40b480e826d9b74143862b64565a4

Ministry of Health Medical Device Manufacturing No. 006546

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Floating Cushion (O.3175)".

o Equipment for physical medicine

O3175 floating seat cushion

Produced in Taiwan, China

Dates and Status

Dec 30, 2016

Dec 30, 2026