Taiwan FDA registration cb0e5227408beb9df18f803dbde29ed5

"Sumi" endotracheal probe (sterilized)

TW: "蘇密"氣管內管探針(滅菌)

Taiwan·Risk Class 1·SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP. K.·Registered May 23, 2018 – May 23, 2023Expired

Registration details

Analysis ID: cb0e5227408beb9df18f803dbde29ed5
Customs Code: DHA09401908506

Company information

Manufacturer: SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP. K.
Manufacturer Country: Poland
Authorized Representative: BIOTRONIC INSTRUMENT ENTERPRISE LTD.

Product details

Intended Use: Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5790 氣管內管探針
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: May 23, 2018
Expiry Date: May 23, 2023

About this record

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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