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"Smith" blood transfusion compression bag (unsterilized) - Taiwan Registration f842ca3d62d8c9b2d2b0b617c56f0ccb

Access comprehensive regulatory information for "Smith" blood transfusion compression 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 f842ca3d62d8c9b2d2b0b617c56f0ccb and manufactured by SMITHS MEDICAL ASD, INC.. The authorized representative in Taiwan is RADIANT MEDICAL COMPANY.

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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f842ca3d62d8c9b2d2b0b617c56f0ccb
Registration Details
Taiwan FDA Registration: f842ca3d62d8c9b2d2b0b617c56f0ccb
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Device Details

"Smith" blood transfusion compression bag (unsterilized)
TW: โ€œๅฒๅฏ†ๆ–ฏโ€ ่ผธ่ก€ๅŠ ๅฃ“่ข‹ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f842ca3d62d8c9b2d2b0b617c56f0ccb

DHA09401592708

Company Information

United States

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

Input;; QMS/QSD

Dates and Status

Dec 03, 2015

Dec 03, 2025