Taiwan FDA registration 255852244d78743519e6e7daceddde38

Guofa urine bag (sterilized)

TW: 國發蓄尿袋(滅菌)

Taiwan·Risk Class 1·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Apr 07, 2006 – Apr 07, 2026Expired

Registration details

Analysis ID: 255852244d78743519e6e7daceddde38
Customs Code: DHY04300117809

Company information

Manufacturer: K.F. MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: K.F. MEDICAL INSTRUMENTS CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.5250 Urine Collector and Accessories Thereof
Import Information: Domestic

Dates and status

Registration Date: Apr 07, 2006
Expiry Date: Apr 07, 2026

About this record

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..

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