Taiwan FDA registration c893649078703a559692648edcd2b814
"Vessel" evoked potential/electromyography instrument
TW: "維塞氏" 誘發電位/肌電圖儀
Registration details
- Analysis ID
- c893649078703a559692648edcd2b814
- Customs Code
- DHA00601162409
Company information
- Manufacturer Country
- United States
- Authorized Representative
- CHANCELLOR INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.1375 診斷用肌電圖儀
- Import Information
- import
Dates and status
- Registration Date
- Jul 25, 2005
- Expiry Date
- Jul 25, 2010
- Cancellation Date
- Nov 23, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Vessel" evoked potential/electromyography instrument in Taiwan's medical device market through Pure Global AI's free database. is registered under number c893649078703a559692648edcd2b814 and manufactured by VIASYS NEUROCARE, A DIV GROUP OF VIASYS HEALTHCARE. The authorized representative in Taiwan is CHANCELLOR INSTRUMENT 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