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"Inte Yakusti" Titan handheld system - Taiwan Registration 6eabc2c89e7633cca01b062a8c6728f0

Access comprehensive regulatory information for "Inte Yakusti" Titan handheld system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6eabc2c89e7633cca01b062a8c6728f0 and manufactured by INTERACOUSTICS A/S. The authorized representative in Taiwan is Baiou Precision Co., Ltd.

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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6eabc2c89e7633cca01b062a8c6728f0
Registration Details
Taiwan FDA Registration: 6eabc2c89e7633cca01b062a8c6728f0
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Device Details

"Inte Yakusti" Titan handheld system
TW: โ€œ้Ÿณ็‰นไบžๅบซๆ–ฏๆโ€ๆณฐๅฆๆ‰‹ๆŒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

6eabc2c89e7633cca01b062a8c6728f0

DHA05602616402

Company Information

Denmark

Product Details

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

K Neuroscience;; G Otolaryngology

G.1050 ่ฝๅŠ›ๆชขๆŸฅ่จˆ;; K.1900 ่ช˜็™ผๅๆ‡‰่ฒๅˆบๆฟ€ๅ™จ

import

Dates and Status

May 13, 2014

May 13, 2019

Jun 16, 2022

Cancellation Information

Logged out

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