Taiwan FDA registration f11462a1009fcb9e7785bec5c8b6df25

"Atrien" chest drainage device (sterilized)

TW: “亞翠恩”胸腔引流器具 (滅菌)

Taiwan·Risk Class 1·Atrium Medical Corporation·Registered Nov 10, 2008 – Nov 10, 2023Expired

Registration details

Analysis ID: f11462a1009fcb9e7785bec5c8b6df25
Customs Code: DHA04400722806

Company information

Manufacturer: Atrium Medical Corporation
Manufacturer Country: United States
Authorized Representative: GETINGE GROUP TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6740 Vacuum-powered fluid absorption apparatus
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Nov 10, 2008
Expiry Date: Nov 10, 2023

About this record

Access comprehensive regulatory information for "Atrien" chest drainage device (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f11462a1009fcb9e7785bec5c8b6df25 and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

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