Pressure device for "Prowei" blood transfusion bag (unsterilized)
Taiwan·Risk Class 1·KAIWEI (SHENZHEN) CO., LTD.·Registered Feb 17, 2014 – Feb 17, 2029Active- Analysis ID
- 81b12774ecfa27db55f8c0c2b0e3ae1d
- Customs Code
- DHA09600207300
- Manufacturer
- KAIWEI (SHENZHEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
- 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
- Chinese goods;; input
- Registration Date
- Feb 17, 2014
- Expiry Date
- Feb 17, 2029
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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.