Taiwan FDA registration c0654a0b0dc07150d9b25d41e0439dbb

"Jiahong" instrument box (unsterilized)

TW: “佳鴻”器械盒 (未滅菌)

Taiwan·Risk Class 1·JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.·Registered Nov 12, 2008 – Nov 12, 2023Expired

Registration details

Analysis ID: c0654a0b0dc07150d9b25d41e0439dbb
Customs Code: DHA04600059208

Company information

Manufacturer: JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.
Manufacturer Country: China
Authorized Representative: CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Chinese goods;; input

Dates and status

Registration Date: Nov 12, 2008
Expiry Date: Nov 12, 2023

About this record

Access comprehensive regulatory information for "Jiahong" instrument box (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0654a0b0dc07150d9b25d41e0439dbb and manufactured by JIN PRAISE MEDICAL TREATMENT INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is CHYA HUNG MEDICAL TREATMENT INSTRUMENTS FACTORY CO., LTD..

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