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Pressure device for "Prowei" blood transfusion bag (unsterilized) - Taiwan Registration 50cb95dd872f17cb65425a32212a0a39

Access comprehensive regulatory information for Pressure device for "Prowei" blood transfusion bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50cb95dd872f17cb65425a32212a0a39 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, 1 companies making similar products including KAIWEI (SHENZHEN) CO., LTD., and 2 recent registrations in the same category. 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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50cb95dd872f17cb65425a32212a0a39
Registration Details
Taiwan FDA Registration: 50cb95dd872f17cb65425a32212a0a39
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Device Details

Pressure device for "Prowei" blood transfusion bag (unsterilized)
TW: โ€œๆ™ฎๅจโ€่ผธ่ก€่ข‹็”จๅฃ“ๅŠ›ๅ™จ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

50cb95dd872f17cb65425a32212a0a39

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the classification and grading management method for medical equipment "Pressure apparatus for intravenous infusion bags (J.5420)".

J General hospital and personal use equipment

J.5420 ้œ่„ˆ่ผธๆถฒ่ข‹็”จๅฃ“ๅŠ›ๅ™จ

Domestic

Dates and Status

Mar 30, 2010

Mar 30, 2025

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