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"Conwilli" Splint for inflated extremities (unsterilized) - Taiwan Registration a300c1e49be4056f43843abaa014aab0

Access comprehensive regulatory information for "Conwilli" Splint for inflated extremities (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a300c1e49be4056f43843abaa014aab0 and manufactured by CONWELL MEDICAL CO., LTD.. The authorized representative in Taiwan is CONWELL MEDICAL 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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a300c1e49be4056f43843abaa014aab0
Registration Details
Taiwan FDA Registration: a300c1e49be4056f43843abaa014aab0
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Device Details

"Conwilli" Splint for inflated extremities (unsterilized)
TW: "ๅบทๅจๅˆฉ" ่†จ่„นๅผๅ››่‚ข็”จๅคพๆฟ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a300c1e49be4056f43843abaa014aab0

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level identification scope of the splint for inflatable limbs (I.3900) in the classification and grading management measures for medical equipment.

I General, Plastic Surgery and Dermatology

I.3900 Clamp board for bulging limbs

Domestic

Dates and Status

Jun 20, 2016

Jun 20, 2026