MYELOTEC, INC.
TaiwanUnited States3 products registeredJul 27, 2012 – Aug 01, 2013
VerifiedTFDA · Taiwan Food and Drug Administration registry
3
Total products
3
Product types
0
Active products
Aug 2013
Latest registration
Company details
- Address
- 4000 NORTHFIELD WAY, STE. 900, ROSWELL, GA 30076, U.S.A.
Regulatory footprint
Search MYELOTEC, INC. across other regulatory registries
Recent 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)
“Myelotec” Flexible Fiberoptic Endoscope & Access Kits
Registered: Aug 01, 2013 • Expires: Aug 01, 2018
Cancelled
- Risk Class
- Class 2
- Type
- MD
- AR
- REVO LASER CORPORATION
"Merotec" image guide tube
Registered: Jul 31, 2012 • Expires: Jul 31, 2022
Cancelled
- Risk Class
- Class 2
- AR
- REVO LASER CORPORATION
"Merotek" Nevix movable catheter
Registered: Jul 27, 2012 • Expires: Jul 27, 2022
Cancelled
- Risk Class
- Class 2
- AR
- REVO LASER CORPORATION
About this profile
Explore comprehensive manufacturer profile for MYELOTEC, INC. based in United States through Pure Global AI's free Taiwan medical device database. This manufacturer has 3 products registered in Taiwan across 3 unique product categories. Their regulatory history spans from Jul 27, 2012 to Aug 01, 2013.
This page provides detailed insights including 3 recent product registrations, 3 most popular products with “Myelotec” Flexible Fiberoptic Endoscope & Access Kits having 1 registrations, and 1 authorized representatives including REVO LASER CORPORATION. Pure Global AI offers free access to Taiwan's medical device database, enabling global MedTech companies to analyze market dynamics and identify opportunities.