Taiwan FDA registration cb2c3d3678da0aaa536cb573d95a1380

"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 Jul 14, 2016 – Jul 14, 2021Expired
Registration details
Analysis ID
cb2c3d3678da0aaa536cb573d95a1380
License Form
Ministry of Health Medical Device Import No. 016780
Customs Code
DHA09401678009
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
Jul 14, 2016
Expiry Date
Jul 14, 2021
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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 cb2c3d3678da0aaa536cb573d95a1380 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, 1 companies making similar products including 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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