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Pressure device for "Prowei" blood transfusion bag (unsterilized) - Taiwan Registration 81b12774ecfa27db55f8c0c2b0e3ae1d

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 81b12774ecfa27db55f8c0c2b0e3ae1d and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Puwei International Co., Ltd. Yilan Factory, 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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81b12774ecfa27db55f8c0c2b0e3ae1d
Registration Details
Taiwan FDA Registration: 81b12774ecfa27db55f8c0c2b0e3ae1d
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Device Details

Pressure device for "Prowei" blood transfusion bag (unsterilized)
TW: "ๆ™ฎๅจ"่ผธ่ก€่ข‹็”จๅฃ“ๅŠ›ๅ™จ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

81b12774ecfa27db55f8c0c2b0e3ae1d

DHA09600207300

Company Information

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

Chinese goods;; input

Dates and Status

Feb 17, 2014

Feb 17, 2029

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