Pure Global

"Medtronic" Indelon second generation laminated stent system - Taiwan Registration 77dda9965126e097909827f5fe3b27aa

Access comprehensive regulatory information for "Medtronic" Indelon second generation laminated stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 77dda9965126e097909827f5fe3b27aa and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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 Database
Powered by Pure Global AI
89,000+ Devices
77dda9965126e097909827f5fe3b27aa
Registration Details
Taiwan FDA Registration: 77dda9965126e097909827f5fe3b27aa
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Medtronic" Indelon second generation laminated stent system
TW: โ€œ็พŽๆ•ฆๅŠ›โ€่Œตๅพทๅ€ซ็ฌฌไบŒไปฃ่ฆ†่†œๆ”ฏๆžถ็ณป็ตฑ
Risk Class 3

Registration Details

77dda9965126e097909827f5fe3b27aa

DHA00602497800

Company Information

Ireland

Product Details

For details Chinese change in the effectiveness of the approved copy of the imitation order: for details, as in the Chinese copy of the imitation order approved copy (the original copy of the imitation label approved copy on December 2, 104 was withdrawn and invalidated).

E Cardiovascular Medicine Science

E.0006.

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Jun 19, 2013

Jun 19, 2028