"Guofa" culture tube (sterilized) - Taiwan Registration 5367c2a3edb11919faeb36cf629eada0
Access comprehensive regulatory information for "Guofa" culture tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5367c2a3edb11919faeb36cf629eada0 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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Device Details
Registration Details
5367c2a3edb11919faeb36cf629eada0
DHY04300169302
Product Details
Limited to the classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
C Immunology and microbiology
C.2900 Microbial sample collection and delivery equipment
Domestic
Dates and Status
Oct 31, 2006
Oct 31, 2026