"Sumi" endotracheal probe (sterilized) - Taiwan Registration cb0e5227408beb9df18f803dbde29ed5
Access comprehensive regulatory information for "Sumi" endotracheal probe (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cb0e5227408beb9df18f803dbde29ed5 and manufactured by SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP. K.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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.
Device Details
Product Details
Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
D Anesthesiology
D.5790 氣管內管探針
QMS/QSD;; 輸入
Dates and Status
May 23, 2018
May 23, 2023

