Taiwan FDA registration a6b8bbd748d8ed2880291b9c80500d9e
Tekmex bone cement mixer (unsterilized)
TW: "泰克美"骨水泥攪拌器(未滅菌)
Taiwan·Risk Class 1·TEKNIMED SAS·Registered May 23, 2013 – May 23, 2018CancelledRegistration details
- Analysis ID
- a6b8bbd748d8ed2880291b9c80500d9e
- Customs Code
- DHA04401304204
Company information
- Manufacturer
- TEKNIMED SAS
- Manufacturer Country
- France
- Authorized Representative
- GREAT UNITED STRONG ENTERPRISE 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
- import
Dates and status
- Registration Date
- May 23, 2013
- Expiry Date
- May 23, 2018
- Cancellation Date
- Oct 02, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Tekmex 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 a6b8bbd748d8ed2880291b9c80500d9e and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..
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