“Wiltrom” Cerapeek Interbody Fusion System - Taiwan Registration 7867aae16d0eb08bb654b5bdd3ac984e
Access comprehensive regulatory information for “Wiltrom” Cerapeek Interbody Fusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7867aae16d0eb08bb654b5bdd3ac984e and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM 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.
Device Details
Registration Details
7867aae16d0eb08bb654b5bdd3ac984e
Ministry of Health Medical Device Manufacturing No. 006512
Product Details
For details, it is Chinese approved copy of the imitation order
N Orthopedic devices
N3080 Interbody fusion device
Produced in Taiwan, China
Dates and Status
Jun 17, 2019
Jun 17, 2024

