Manufacturer profileJOTEC GmbH
TaiwanGermany4 products registeredDec 10, 2014 – Nov 26, 2024
VerifiedTFDA · Taiwan Food and Drug Administration registry
4
Total products
4
Product types
2
Active products
Nov 2024
Latest registration
Company details
- Address
- Lotzenacker 23, 72379 Hechingen Germany
Regulatory footprint
Search JOTEC GmbH across other regulatory registries
Thailand
European Union
Colombia
South Korea
Canada
EcuadorRecent registrations
Latest 5 products registered by this manufacturer
Most popular products
Products with most registrations
Authorized representatives
Taiwan authorized representatives for this manufacturer
Recent registered products
Most recent products (showing top 20)
"UDEK" Itag stent graft system
Registered: Nov 26, 2024 • Expires: Nov 26, 2029
- Risk Class
- Class 3
- AR
- EMERGO TAIWAN LIMITED
“Jotec” E-wire Guide Wire
Registered: Feb 23, 2021 • Expires: Feb 23, 2026
- Risk Class
- Class 2
- Type
- MD
- AR
- EMERGO TAIWAN LIMITED
“E-WIRE” GUIDE WIRE
Registered: Apr 24, 2015 • Expires: Apr 24, 2020
Cancelled
- Risk Class
- Class 2
- Type
- MD
- AR
- LEIN YIH MEDICAL CO.
“E-VITA” OPEN PLUS STENT GRAFT SYSTEM
Registered: Dec 10, 2014 • Expires: Dec 10, 2019
Cancelled
- Risk Class
- Class 3
- Type
- MD
- AR
- LEIN YIH MEDICAL CO.
About this profile
Explore comprehensive manufacturer profile for JOTEC GmbH based in Germany through Pure Global AI's free Taiwan medical device database. This manufacturer has 4 products registered in Taiwan across 4 unique product categories. Their regulatory history spans from Dec 10, 2014 to Nov 26, 2024.
This page provides detailed insights including 4 recent product registrations, 4 most popular products with "UDEK" Itag stent graft system having 1 registrations, and 2 authorized representatives including EMERGO TAIWAN LIMITED. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.