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Kangyang air cushion (unsterilized) - Taiwan Registration a2a64c7caa6d54c5d6e7ed4669f70b5b

Access comprehensive regulatory information for Kangyang air cushion (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a2a64c7caa6d54c5d6e7ed4669f70b5b and manufactured by VICAIR BV. The authorized representative in Taiwan is KARMA MEDICAL PRODUCTS 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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a2a64c7caa6d54c5d6e7ed4669f70b5b
Registration Details
Taiwan FDA Registration: a2a64c7caa6d54c5d6e7ed4669f70b5b
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Device Details

Kangyang air cushion (unsterilized)
TW: ๅบทๆšๆฐฃๅขŠ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a2a64c7caa6d54c5d6e7ed4669f70b5b

DHA04400362305

Company Information

Netherlands

Product Details

Limited to the first level identification scope of the "floating cushion (O.3175)" of the Measures for the Classification and Grading Management of Medical Equipment.

o Physical Medical Sciences

O.3175 Floating cushion

import

Dates and Status

Apr 12, 2006

Apr 12, 2026