Taiwan FDA registration 8722822cda6cd3fd0519c1ccd8ea9a61

Linqi vertebral bone cement

TW: 琳悧椎體骨水泥
Taiwan flagTaiwan·Risk Class 2·ZHENPENG BIOTECH CO., LTD.·Registered Aug 31, 2019 – Jul 10, 2028Active
Registration details
Analysis ID
8722822cda6cd3fd0519c1ccd8ea9a61
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
LINLI CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3027 PMMA骨水泥
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Aug 31, 2019
Expiry Date
Jul 10, 2028
About this record

Access comprehensive regulatory information for Linqi vertebral 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 8722822cda6cd3fd0519c1ccd8ea9a61 and manufactured by ZHENPENG BIOTECH CO., LTD.. The authorized representative in Taiwan is LINLI 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 DatabasePowered by Pure Global AI89,000+ Devices