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"Sivantos" A & M Hearing Aid (Non-Sterile) - Taiwan Registration cb2c3d3678da0aaa536cb573d95a1380

Access comprehensive regulatory information for "Sivantos" A & M 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 cb2c3d3678da0aaa536cb573d95a1380 and manufactured by SIVANTOS PTE LTD. The authorized representative in Taiwan is KING PAX TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIVANTOS PTE. LTD, and 2 recent registrations in the same category. 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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Registration Details
Taiwan FDA Registration: cb2c3d3678da0aaa536cb573d95a1380
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Device Details

"Sivantos" A & M Hearing Aid (Non-Sterile)
TW: "่ฅฟ่ฌๆ‹“" ๆ„›็พŽๅŠฉ่ฝๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

cb2c3d3678da0aaa536cb573d95a1380

Ministry of Health Medical Device Import No. 016780

DHA09401678009

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

Jul 14, 2016

Jul 14, 2021

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