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Guofa urine bag (sterilized) - Taiwan Registration 255852244d78743519e6e7daceddde38

Access comprehensive regulatory information for Guofa urine bag (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 255852244d78743519e6e7daceddde38 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..

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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255852244d78743519e6e7daceddde38
Registration Details
Taiwan FDA Registration: 255852244d78743519e6e7daceddde38
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Device Details

Guofa urine bag (sterilized)
TW: ๅœ‹็™ผ่“„ๅฐฟ่ข‹(ๆป…่Œ)
Risk Class 1

Registration Details

255852244d78743519e6e7daceddde38

DHY04300117809

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "urine collector and its accessories (H.5250)" of the Measures for the Classification and Grading Management of Medical Devices.

H Gastroenterology and urology

H.5250 Urine Collector and Accessories Thereof

Domestic

Dates and Status

Apr 07, 2006

Apr 07, 2026