Taiwan FDA registration 1036fd4ba1de4532cb8d0d6944a29741

"Miesio" non-powered neurosurgical instruments (unsterilized)

TW: “密斯奧” 非動力式神經外科用器械（未滅菌）

Taiwan·Risk Class 1·MIZUHO AMERICA, INC.·Registered Nov 25, 2009 – Nov 25, 2014Cancelled

Registration details

Analysis ID: 1036fd4ba1de4532cb8d0d6944a29741
Customs Code: DHA04400831700

Company information

Manufacturer: MIZUHO AMERICA, INC.
Manufacturer Country: United States
Authorized Representative: BARRY TEC ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Neurosurgical Devices (K.4535)".
Product Type (Level 1): K Neuroscience
Product Type (Level 2): K.4535 非動力式神經外科用器械
Import Information: import

Dates and status

Registration Date: Nov 25, 2009
Expiry Date: Nov 25, 2014
Cancellation Date: Aug 09, 2018

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Miesio" non-powered neurosurgical instruments (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1036fd4ba1de4532cb8d0d6944a29741 and manufactured by MIZUHO AMERICA, INC.. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..

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