Taiwan FDA registration d034086f06925c28372f85cd49ef8991

"Shanghai Optoelectronics" blood cell diluent (unsterilized)

TW: "上海光電" 血球稀釋劑 (未滅菌)

Taiwan·Risk Class 1·SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.·Registered Nov 19, 2019 – Nov 19, 2024Expired

Registration details

Analysis ID: d034086f06925c28372f85cd49ef8991
Customs Code: DHA09600401700

Company information

Manufacturer: SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.
Manufacturer Country: China
Authorized Representative: CHFO BIOMED CORP.

Product details

Intended Use: Limited to the first level identification range of "blood cell thinners (B.8200)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.8200 Hemocytodilant
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Nov 19, 2019
Expiry Date: Nov 19, 2024

About this record

Access comprehensive regulatory information for "Shanghai Optoelectronics" blood cell diluent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d034086f06925c28372f85cd49ef8991 and manufactured by SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.. The authorized representative in Taiwan is CHFO BIOMED CORP..

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