Pure Global

"Kawi" fiber optic laryngoscope - Taiwan Registration f74170adb397fa3eca12e27e286eee81

Access comprehensive regulatory information for "Kawi" fiber optic laryngoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f74170adb397fa3eca12e27e286eee81 and manufactured by KIRCHNER & WILHELM GMBH CO. KG. The authorized representative in Taiwan is DURAMED INTERNATIONAL CORPORATION.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
f74170adb397fa3eca12e27e286eee81
Registration Details
Taiwan FDA Registration: f74170adb397fa3eca12e27e286eee81
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kawi" fiber optic laryngoscope
TW: "ๅกๅจ" ๅ…‰็บ–ๅ–‰้ ญ้ก
Risk Class 1
Cancelled

Registration Details

f74170adb397fa3eca12e27e286eee81

DHA04400031100

Company Information

Product Details

Inspect and review the patient's upper airway and assist in endotracheal tube placement.

D Anesthesiology

import

Dates and Status

Aug 10, 2005

Aug 10, 2010

May 20, 2011

Cancellation Information

Logged out

่‡ช่ซ‹่จป้Šท