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Taiwan FDA registration cb3bc44ff2c0b1549996e40407a5cbf6

"Vessel" electrode wire (unsterilized)

TW: “維塞氏”電極線 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·VIASYS NEUROCARE, A DIV GROUP OF VIASYS HEALTHCARE·Registered Oct 22, 2007 – Oct 22, 2012Cancelled
Registration details
Analysis ID
cb3bc44ff2c0b1549996e40407a5cbf6
Customs Code
DHA04400623205
Company information
Manufacturer
VIASYS NEUROCARE, A DIV GROUP OF VIASYS HEALTHCARE
Manufacturer Country
United States
Authorized Representative
CHANCELLOR INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification range of electrode wire (O.1175) of the medical device management method.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.1175 Electrode wire
Import Information
import
Dates and status
Registration Date
Oct 22, 2007
Expiry Date
Oct 22, 2012
Cancellation Date
Apr 30, 2014
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Vessel" electrode wire (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb3bc44ff2c0b1549996e40407a5cbf6 and manufactured by VIASYS NEUROCARE, A DIV GROUP OF VIASYS HEALTHCARE. The authorized representative in Taiwan is CHANCELLOR INSTRUMENT CO., LTD..

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