Taiwan FDA registration c8a2e025f9f76157cfffccf032f8d45d

Fully sterilized (unsterilized)

TW: 全滅菌 (未滅菌)

Taiwan·Risk Class 1·GINYORK MFG. CO., LTD.·Registered Nov 10, 2005 – Nov 10, 2010Cancelled

Registration details

Analysis ID: c8a2e025f9f76157cfffccf032f8d45d
Customs Code: DHY04300068202

Company information

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

Product details

Intended Use: It is used for the pre-washing and decontamination of non-hazardous medical devices and equipment surfaces, and for the final sterilization or high disinfection of dangerous or semi-dangerous medical devices.
Product Type (Level 1): J General hospital and personal use equipment
Import Information: Domestic

Dates and status

Registration Date: Nov 10, 2005
Expiry Date: Nov 10, 2010
Cancellation Date: Apr 30, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Fully sterilized (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c8a2e025f9f76157cfffccf032f8d45d and manufactured by GINYORK MFG. CO., LTD.. The authorized representative in Taiwan is GINYORK MFG. CO., LTD..

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