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"Prowei" chest drainage bottle (sterilized) - Taiwan Registration 2d8327c6f6acf8a443e75ac715923285

Access comprehensive regulatory information for "Prowei" chest drainage bottle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2d8327c6f6acf8a443e75ac715923285 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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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2d8327c6f6acf8a443e75ac715923285
Registration Details
Taiwan FDA Registration: 2d8327c6f6acf8a443e75ac715923285
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Device Details

"Prowei" chest drainage bottle (sterilized)
TW: "ๆ™ฎๅจ" ่ƒธ่…”ๅผ•ๆต็“ถ (ๆป…่Œ)
Risk Class 1

Registration Details

2d8327c6f6acf8a443e75ac715923285

Company Information

Taiwan, Province of China

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

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Dec 21, 2016

Dec 21, 2026