Taiwan FDA registration fedcbc3f601467ac2eaa5f10a75bcc9d

"SiemensBayaudio" Hearing aids (Non-Sterile)

TW: "西門子聽貝爾" 助聽器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·SIVANTOS PTE. LTD·Registered Dec 01, 2017 – Dec 01, 2027Active
Registration details
Analysis ID
fedcbc3f601467ac2eaa5f10a75bcc9d
License Form
Ministry of Health Medical Device Import No. 018565
Customs Code
DHA09401856502
Company information
Manufacturer
SIVANTOS PTE. LTD
Manufacturer Country
Singapore
Authorized Representative
BAY AUDIOLOGY (TAIWAN) LIMITED
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 01, 2017
Expiry Date
Dec 01, 2027
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About this record

Access comprehensive regulatory information for "SiemensBayaudio" Hearing aids (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 fedcbc3f601467ac2eaa5f10a75bcc9d and manufactured by SIVANTOS PTE. LTD. The authorized representative in Taiwan is BAY AUDIOLOGY (TAIWAN) LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIVANTOS PTE LTD, and 1 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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