Pure Global

“Orthobion” TSC Posterior/ Transforaminal Lumbar Interbody Fusion Cages - Taiwan Registration 1201fb1cb999a4e1e7c915e23a4601f2

Access comprehensive regulatory information for “Orthobion” TSC Posterior/ Transforaminal Lumbar Interbody Fusion Cages in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1201fb1cb999a4e1e7c915e23a4601f2 and manufactured by Orthobion GmbH. The authorized representative in Taiwan is LI MIN BIOTECH 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
1201fb1cb999a4e1e7c915e23a4601f2
Registration Details
Taiwan FDA Registration: 1201fb1cb999a4e1e7c915e23a4601f2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Orthobion” TSC Posterior/ Transforaminal Lumbar Interbody Fusion Cages
TW: “歐梭比恩”腰椎後側路椎間融合器
Risk Class 2
MD

Registration Details

1201fb1cb999a4e1e7c915e23a4601f2

Ministry of Health Medical Device Import No. 032991

DHA05603299107

Company Information

Germany

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Nov 10, 2019

Nov 10, 2024