Pure Global

"Karlsted" electronic mediastinoscope - Taiwan Registration b08d33c8b86932538e49a0f70eae8c41

Access comprehensive regulatory information for "Karlsted" electronic mediastinoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b08d33c8b86932538e49a0f70eae8c41 and manufactured by Karl Storz SE & Co. KG. The authorized representative in Taiwan is KARL STORZ ENDOSCOPY TAIWAN 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
b08d33c8b86932538e49a0f70eae8c41
Registration Details
Taiwan FDA Registration: b08d33c8b86932538e49a0f70eae8c41
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Karlsted" electronic mediastinoscope
TW: โ€œๅก็ˆพๆ–ฏ็‰นโ€้›ปๅญๅผ็ธฑ่†ˆ่…”้ก
Risk Class 2

Registration Details

b08d33c8b86932538e49a0f70eae8c41

DHA05603517100

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

G ENT Science

G.4720 Diaphragmatic cavity mirrors and accessories

import

Dates and Status

Jan 04, 2022

Jan 04, 2027