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"Pulton" air-guided hearing aids (unsterilized) - Taiwan Registration 9a85cf2d2e44c11472bc038530e805da

Access comprehensive regulatory information for "Pulton" air-guided hearing aids (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9a85cf2d2e44c11472bc038530e805da and manufactured by PURETONE LTD.. The authorized representative in Taiwan is JEN SOUND ENTERPRISE 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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9a85cf2d2e44c11472bc038530e805da
Registration Details
Taiwan FDA Registration: 9a85cf2d2e44c11472bc038530e805da
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Device Details

"Pulton" air-guided hearing aids (unsterilized)
TW: โ€œๆ™ฎ่€ณ้€šโ€ๆฐฃๅฐŽๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

9a85cf2d2e44c11472bc038530e805da

DHA04400749302

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".

G ENT Science

G.3300 Hearing Aids

import

Dates and Status

Feb 17, 2009

Feb 17, 2014

Jan 09, 2017

Cancellation Information

Logged out

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