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"Sivantos" A & M Hearing Aid (Non-Sterile) - Taiwan Registration 0c1ffc1f053e4a8a3b124653718d9ea6

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 0c1ffc1f053e4a8a3b124653718d9ea6 and manufactured by SIVANTOS PTE. LTD. The authorized representative in Taiwan is Faciox Inc..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including SIVANTOS PTE LTD, 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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0c1ffc1f053e4a8a3b124653718d9ea6
Registration Details
Taiwan FDA Registration: 0c1ffc1f053e4a8a3b124653718d9ea6
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Device Details

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

Registration Details

0c1ffc1f053e4a8a3b124653718d9ea6

Ministry of Health Medical Device Import No. 020410

DHA09402041004

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 06, 2019

May 06, 2024

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