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"Signia" Hearing Aid (Non-Sterile) - Taiwan Registration 922b130837062578846e920dcc892d3a

Access comprehensive regulatory information for "Signia" Hearing Aid (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 922b130837062578846e920dcc892d3a and manufactured by SIVANTOS PTE LTD. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.

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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922b130837062578846e920dcc892d3a
Registration Details
Taiwan FDA Registration: 922b130837062578846e920dcc892d3a
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Device Details

"Signia" Hearing Aid (Non-Sterile)
TW: "่ฅฟๅ˜‰" ๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

922b130837062578846e920dcc892d3a

Ministry of Health Medical Device Import No. 020521

DHA09402052100

Company Information

Singapore

Product Details

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

G ENT device

G3300 hearing aid

Imported from abroad

Dates and Status

Jun 04, 2019

Jun 04, 2024