Catheter Guide, 450 x Ф2.5 - FDA Registration c00365e9b661a1c7f9a5d872d0a0d928
Access comprehensive regulatory information for Catheter Guide, 450 x Ф2.5 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c00365e9b661a1c7f9a5d872d0a0d928 and manufactured by Xinhua Surgical Instruments Co. Ltd. The device was registered on August 05, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
Free Database
Powered by Pure Global AI
FDA Official Data
c00365e9b661a1c7f9a5d872d0a0d928
Catheter Guide, 450 x Ф2.5
FDA ID: c00365e9b661a1c7f9a5d872d0a0d928
Device Classification
Brand Name
SHINVA
Registration Information
Analysis ID
c00365e9b661a1c7f9a5d872d0a0d928
Registration Date
August 05, 2022
Manufacturer
Authorized Representative

