Taiwan FDA registration 50cb95dd872f17cb65425a32212a0a39

Pressure device for "Prowei" blood transfusion bag (unsterilized)

TW: “普威”輸血袋用壓力器(未滅菌)
Taiwan flagTaiwan·Risk Class 1·Puwei International Co., Ltd. Yilan Factory·Registered Mar 30, 2010 – Mar 30, 2025Expired
Registration details
Analysis ID
50cb95dd872f17cb65425a32212a0a39
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
UNIMAX MEDICAL SYSTEMS INC.
Product details
Intended Use
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)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5420 靜脈輸液袋用壓力器
Import Information
Domestic
Dates and status
Registration Date
Mar 30, 2010
Expiry Date
Mar 30, 2025
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About this record

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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