Taiwan FDA registration e55b60c81912fe428345b452e2cee95b

"Schumak" bone cement dispenser (sterilization)

TW: “舒馬克”骨水泥分配器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·SOMATEX MEDICAL TECHNOLOGIES GMBH·Registered Feb 11, 2009 – Feb 11, 2014Cancelled
Registration details
Analysis ID
e55b60c81912fe428345b452e2cee95b
Customs Code
DHA04400746701
Company information
Manufacturer Country
Germany
Authorized Representative
Zhaofeng Biotechnology Co., Ltd
Product details
Intended Use
Limited to the first level identification range of the bone cement dispenser (N.4200) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.4200 Bone cement distributor
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Feb 11, 2009
Expiry Date
Feb 11, 2014
Cancellation Date
Dec 14, 2016
Cancellation information
Status
Logged out
Reason
屆期未申請展延
About this record

Access comprehensive regulatory information for "Schumak" bone cement dispenser (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e55b60c81912fe428345b452e2cee95b and manufactured by SOMATEX MEDICAL TECHNOLOGIES GMBH. The authorized representative in Taiwan is Zhaofeng Biotechnology 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