Taiwan FDA registration 41b58d59d1faea0790c9d287885a3cdd

"Fengsheng" instrument loading box (unsterilized)

TW: "豐生" 器械裝載盒 (未滅菌)

Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Feb 13, 2018 – Feb 13, 2023Expired

Registration details

Analysis ID: 41b58d59d1faea0790c9d287885a3cdd

Company information

Manufacturer: DI CHENG RUBBER INDUSTRIES INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HONG SHENG MEDICAL INSTRUMENTS CO.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Domestic;; Contract manufacturing

Dates and status

Registration Date: Feb 13, 2018
Expiry Date: Feb 13, 2023

About this record

Access comprehensive regulatory information for "Fengsheng" instrument loading 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 41b58d59d1faea0790c9d287885a3cdd and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is HONG SHENG MEDICAL INSTRUMENTS CO..

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