Pure Global

"Fujino" bronchoscope - Taiwan Registration 179ec77a25276e5592ff8a8d0c73e21e

Access comprehensive regulatory information for "Fujino" bronchoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 179ec77a25276e5592ff8a8d0c73e21e and manufactured by FUJINON MITO CORPORATION. The authorized representative in Taiwan is WELMORE 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
179ec77a25276e5592ff8a8d0c73e21e
Registration Details
Taiwan FDA Registration: 179ec77a25276e5592ff8a8d0c73e21e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Fujino" bronchoscope
TW: "ๅฏŒๅฃซ่ƒฝ" ๆ”ฏๆฐฃ็ฎก้ก
Risk Class 2
Cancelled

Registration Details

179ec77a25276e5592ff8a8d0c73e21e

DHA00601357802

Company Information

Japan

Product Details

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

G ENT Science

G.4680 Bronchial tubescopes (soft or rigid) and accessories thereof

import

Dates and Status

Nov 17, 2005

Nov 17, 2020

Jun 22, 2022

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ