Taiwan FDA registration eacb732577a9db0e299bb0bece8a5274

"Zhengyang" bone cement mixer (unsterilized)

TW: "正揚"骨水泥攪拌器(未滅菌)

Taiwan·Risk Class 1·ZHENG YANG BIOMEDICAL TECHNOLOGY CO., LTD.·Registered Apr 21, 2010 – Apr 21, 2015Cancelled

Registration details

Analysis ID: eacb732577a9db0e299bb0bece8a5274

Company information

Manufacturer: ZHENG YANG BIOMEDICAL TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: ZHENG YANG BIOMEDICAL TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Clinical Bone Cement Mixer (N.4210)".
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4210 臨床用骨水泥攪拌器
Import Information: Domestic

Dates and status

Registration Date: Apr 21, 2010
Expiry Date: Apr 21, 2015
Cancellation Date: Aug 14, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Zhengyang" bone cement mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number eacb732577a9db0e299bb0bece8a5274 and manufactured by ZHENG YANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is ZHENG YANG BIOMEDICAL TECHNOLOGY 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.