Taiwan FDA registration 8f6f553d7bfa6dc482067f9e20166a08
"Novarterk" intra-contrast imaging system
TW: “諾華德克”史拜術中造影系統
Registration details
- Analysis ID
- 8f6f553d7bfa6dc482067f9e20166a08
- Customs Code
- DHA00602138408
Company information
- Manufacturer
- NOVADAQ TECHNOLOGIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- KINGDOM EAST ENTERPRISE CO., LTD.
Product details
- Intended Use
- Fluorescence imaging is used to visually evaluate the qualitative perfusion of blood flow in the tissues associated with coronary artery bypass surgery.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1600 X光血管攝影系統
- Import Information
- import
Dates and status
- Registration Date
- Sep 16, 2010
- Expiry Date
- Sep 16, 2015
- 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 "Novarterk" intra-contrast imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f6f553d7bfa6dc482067f9e20166a08 and manufactured by NOVADAQ TECHNOLOGIES INC.. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE 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