Taiwan FDA registration 5367c2a3edb11919faeb36cf629eada0

"Guofa" culture tube (sterilized)

TW: “國發”培養管(滅菌)

Taiwan·Risk Class 1·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Oct 31, 2006 – Oct 31, 2026Active

Registration details

Analysis ID: 5367c2a3edb11919faeb36cf629eada0
Customs Code: DHY04300169302

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 classification and grading management measures for medical equipment "Microbial Sample Collection and Delivery Equipment (C.2900)" the first level identification range.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2900 Microbial sample collection and delivery equipment
Import Information: Domestic

Dates and status

Registration Date: Oct 31, 2006
Expiry Date: Oct 31, 2026

About this record

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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