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"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..

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cb0e5227408beb9df18f803dbde29ed5
Registration Details
Taiwan FDA Registration: cb0e5227408beb9df18f803dbde29ed5
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Device Details

"Sumi" endotracheal probe (sterilized)
TW: "蘇密"氣管內管探針(滅菌)
Risk Class 1

Registration Details

cb0e5227408beb9df18f803dbde29ed5

DHA09401908506

Company Information

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