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"Prowei" closed suction sleeve (sterilized) - Taiwan Registration a03b7be526691d35a1c8ee620b6801c7

Access comprehensive regulatory information for "Prowei" closed suction sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a03b7be526691d35a1c8ee620b6801c7 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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a03b7be526691d35a1c8ee620b6801c7
Registration Details
Taiwan FDA Registration: a03b7be526691d35a1c8ee620b6801c7
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Device Details

"Prowei" closed suction sleeve (sterilized)
TW: โ€œๆ™ฎๅจโ€ๅฏ†้–‰ๅผๆŠฝ็—ฐๅฅ— (ๆป…่Œ)
Risk Class 1

Registration Details

a03b7be526691d35a1c8ee620b6801c7

Company Information

Taiwan, Province of China

Product Details

Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.

D Anesthesiology

D.6810 Pneumatic bronchial suction guide tube

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jun 22, 2010

Jun 22, 2025