Pure Global

“G-21” V-Steady Bone Cement - Taiwan Registration b95473f3eb368fad752d111fb17e176c

Access comprehensive regulatory information for “G-21” V-Steady Bone Cement in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b95473f3eb368fad752d111fb17e176c and manufactured by G-21 S.r.l. The authorized representative in Taiwan is SUMMIT BIOMED. 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
b95473f3eb368fad752d111fb17e176c
Registration Details
Taiwan FDA Registration: b95473f3eb368fad752d111fb17e176c
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“G-21” V-Steady Bone Cement
TW: “脊而益”穩固椎體成形術高黏度骨水泥
Risk Class 2
MD

Registration Details

b95473f3eb368fad752d111fb17e176c

Ministry of Health Medical Device Import No. 034268

DHA05603426807

Company Information

Italy

Product Details

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

N Orthopedic devices

N3027 PMMA bone cement

Imported from abroad

Dates and Status

Jan 22, 2021

Jan 22, 2026