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VenAir Sequential Compression System - Taiwan Registration cdb98ef10f5c68d9b0bae07875ad9a8c

Access comprehensive regulatory information for VenAir Sequential Compression System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cdb98ef10f5c68d9b0bae07875ad9a8c and manufactured by Wellell Inc.. The authorized representative in Taiwan is Wellell Inc..

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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Registration Details
Taiwan FDA Registration: cdb98ef10f5c68d9b0bae07875ad9a8c
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Device Details

VenAir Sequential Compression System
TW: โ€œ้›ƒๅšโ€้€ฃ็บŒๅŠ ๅฃ“็ณป็ตฑ
Risk Class 2
MD

Registration Details

cdb98ef10f5c68d9b0bae07875ad9a8c

Ministry of Health Medical Device Manufacturing No. 007457

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E5800 Compression sleeve for extremities

Produced in Taiwan, China

Dates and Status

Apr 20, 2022

Apr 20, 2027