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"REXTON" Hearing Aid (Non-Sterile) - Taiwan Registration 230ee301c85077ce18d7904e7218a1d2

Access comprehensive regulatory information for "REXTON" 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 230ee301c85077ce18d7904e7218a1d2 and manufactured by SIVANTOS PTE. LTD. The authorized representative in Taiwan is CLINICO 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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230ee301c85077ce18d7904e7218a1d2
Registration Details
Taiwan FDA Registration: 230ee301c85077ce18d7904e7218a1d2
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Device Details

"REXTON" Hearing Aid (Non-Sterile)
TW: "้›ทๆ–ฏ้ “" ๅŠฉ่ฝๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

230ee301c85077ce18d7904e7218a1d2

Ministry of Health Medical Device Import No. 019039

DHA09401903902

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

May 11, 2018

May 11, 2028