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"Atrien" chest drainage device (sterilized) - Taiwan Registration f11462a1009fcb9e7785bec5c8b6df25

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..

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.

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f11462a1009fcb9e7785bec5c8b6df25
Registration Details
Taiwan FDA Registration: f11462a1009fcb9e7785bec5c8b6df25
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Device Details

"Atrien" chest drainage device (sterilized)
TW: โ€œไบž็ฟ ๆฉโ€่ƒธ่…”ๅผ•ๆตๅ™จๅ…ท (ๆป…่Œ)
Risk Class 1

Registration Details

f11462a1009fcb9e7785bec5c8b6df25

DHA04400722806

Company Information

United States

Product Details

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)".

J General hospital and personal use equipment

J.6740 Vacuum-powered fluid absorption apparatus

Input;; QMS/QSD

Dates and Status

Nov 10, 2008

Nov 10, 2023