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"Indeku" Anfei hearing aid analysis system and its accessories - Taiwan Registration 12dc92ed309ce32f8b16b5ed106ae81d

Access comprehensive regulatory information for "Indeku" Anfei hearing aid analysis system and its accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12dc92ed309ce32f8b16b5ed106ae81d and manufactured by INTERACOUSTICS A/S. The authorized representative in Taiwan is CLINICO INC..

This page provides complete technical specifications, regulatory compliance details. 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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12dc92ed309ce32f8b16b5ed106ae81d
Registration Details
Taiwan FDA Registration: 12dc92ed309ce32f8b16b5ed106ae81d
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Device Details

"Indeku" Anfei hearing aid analysis system and its accessories
TW: โ€œ่‹ฑๅพทๅบซโ€ๅฎ‰้ฃ›ๅŠฉ่ฝๅ™จๅˆ†ๆž็ณป็ตฑๅŠๅ…ถ้™„ไปถ
Risk Class 2

Registration Details

12dc92ed309ce32f8b16b5ed106ae81d

DHA05603381505

Company Information

Denmark

Product Details

For details, it is Chinese approved copy of the imitation order

G ENT Science

G.1050 ่ฝๅŠ›ๆชขๆŸฅ่จˆ;; G.3310 ๅŠฉ่ฝๅ™จๆ กๆญฃๅ™จๅŠๅˆ†ๆž็ณป็ตฑ

import

Dates and Status

Jul 25, 2020

Jul 25, 2025