Taiwan FDA registration 9d47c83b9c6b6b1e36ef7944c836e2ed

"Jiahong" drip rack (unsterilized)

TW: “佳鴻”點滴架 (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: 9d47c83b9c6b6b1e36ef7944c836e2ed
Customs Code: DHA04600059300

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 range of the "Injection Rack (J.6990)" of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6990 Injection holder
Import Information: Input;; Chinese goods

Dates and status

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

About this record

Access comprehensive regulatory information for "Jiahong" drip rack (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9d47c83b9c6b6b1e36ef7944c836e2ed 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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