Taiwan FDA registration b1e188087e464dba4e42c44952a5f74a

Must be sterilized Disinfectant for general medical devices (unsterilized)

TW: 必滅菌一般醫療器械用消毒劑(未滅菌)

Taiwan·Risk Class 1·GINYORK MFG. CO., LTD.·Registered Apr 28, 2011 – Apr 28, 2026Expired

Registration details

Analysis ID: b1e188087e464dba4e42c44952a5f74a

Company information

Manufacturer: GINYORK MFG. CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: GINYORK MFG. CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.6890 Disinfectants for general medical equipment
Import Information: Domestic

Dates and status

Registration Date: Apr 28, 2011
Expiry Date: Apr 28, 2026

About this record

Access comprehensive regulatory information for Must be sterilized Disinfectant for general medical devices (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b1e188087e464dba4e42c44952a5f74a and manufactured by GINYORK MFG. CO., LTD.. The authorized representative in Taiwan is GINYORK MFG. CO., LTD..

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