Taiwan FDA registration c51bacacd2b96de1e303115d90cc3331

"Sumi" respirator tubing (sterilized)

TW: "蘇密"呼吸器管路(滅菌)

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

Registration details

Analysis ID: c51bacacd2b96de1e303115d90cc3331
Customs Code: DHA09401908608

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 identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5975 Respirator Tubing
Import Information: Input;; QMS/QSD

Dates and status

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

About this record

Access comprehensive regulatory information for "Sumi" respirator tubing (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c51bacacd2b96de1e303115d90cc3331 and manufactured by SUMI SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ SP. K.. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

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