Taiwan FDA registration d08a318615f2d8fd8de221f55a47f9c7

"Guofa" three-piece dental kit (sterilized)

TW: "國發" 三件組牙科包 (滅菌)

Taiwan·Risk Class 1·K.F. MEDICAL INSTRUMENTS CO., LTD.·Registered Nov 28, 2006 – Nov 28, 2026Active

Registration details

Analysis ID: d08a318615f2d8fd8de221f55a47f9c7
Customs Code: DHY04300172104

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 of medical equipment, the first level identification range of dental hand instruments (F.4565).
Product Type (Level 1): F Dentistry
Product Type (Level 2): F.4565 牙科手用器械
Import Information: Domestic

Dates and status

Registration Date: Nov 28, 2006
Expiry Date: Nov 28, 2026

About this record

Access comprehensive regulatory information for "Guofa" three-piece dental kit (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d08a318615f2d8fd8de221f55a47f9c7 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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