Taiwan FDA registration eb542cc1823fe4c9749eb8a96f2ac1e7

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

TW: "西萬拓" 愛美助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SIVANTOS PTE. LTD·Registered Dec 22, 2017 – Dec 22, 2027Active
Registration details
Analysis ID
eb542cc1823fe4c9749eb8a96f2ac1e7
License Form
Ministry of Health Medical Device Import No. 018639
Customs Code
DHA09401863905
Company information
Manufacturer
SIVANTOS PTE. LTD
Manufacturer Country
Singapore
Authorized Representative
KING PAX TECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Hearing Aids (G.3300)".
Product Type (Level 1)
G ENT device
Product Type (Level 2)
G3300 hearing aid
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 22, 2017
Expiry Date
Dec 22, 2027
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About this record

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 eb542cc1823fe4c9749eb8a96f2ac1e7 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, 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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