Taiwan FDA registration a807d18b6364e423aeb883e00c192202

"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 Sep 20, 2017 – Sep 20, 2022Expired
Registration details
Analysis ID
a807d18b6364e423aeb883e00c192202
License Form
Ministry of Health Medical Device Import No. 018337
Customs Code
DHA09401833702
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
Sep 20, 2017
Expiry Date
Sep 20, 2022
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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 a807d18b6364e423aeb883e00c192202 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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