Taiwan FDA registration 0c1ffc1f053e4a8a3b124653718d9ea6

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

TW: "西萬拓" 艾曼助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SIVANTOS PTE. LTD·Registered May 06, 2019 – May 06, 2024Expired
Registration details
Analysis ID
0c1ffc1f053e4a8a3b124653718d9ea6
License Form
Ministry of Health Medical Device Import No. 020410
Customs Code
DHA09402041004
Company information
Manufacturer
SIVANTOS PTE. LTD
Manufacturer Country
Singapore
Authorized Representative
Faciox Inc.
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
May 06, 2019
Expiry Date
May 06, 2024
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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 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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