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“KADEN” Video Intubation Flexible Laryngoscope (Non-Sterile) - Taiwan Registration f95399158bd7c70fb0b959866447e246

Access comprehensive regulatory information for “KADEN” Video Intubation Flexible Laryngoscope (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 f95399158bd7c70fb0b959866447e246 and manufactured by KADEN INTERNATIONAL LTD.. The authorized representative in Taiwan is PRO-READY ENTERPRISE 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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f95399158bd7c70fb0b959866447e246
Registration Details
Taiwan FDA Registration: f95399158bd7c70fb0b959866447e246
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Device Details

“KADEN” Video Intubation Flexible Laryngoscope (Non-Sterile)
TW: “卡德”電子影像喉頭鏡 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

f95399158bd7c70fb0b959866447e246

Ministry of Health Medical Device Import No. 014111

DHA09401411108

Company Information

Hong Kong

Product Details

D Devices for anesthesiology

D5530 Flexible laryngoscope

Imported from abroad

Dates and Status

May 06, 2014

May 06, 2019

Jun 16, 2022

Cancellation Information

Logged out

許可證已逾有效期未申請展延