Taiwan FDA registration c26e5cfd27973847a50f98141d6129a5

"Shanghai Optoelectronics" erythrocytolytic agent (unsterilized)

TW: "上海光電" 紅血球溶解劑 (未滅菌)

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

Registration details

Analysis ID: c26e5cfd27973847a50f98141d6129a5
Customs Code: DHA09600401802

Company information

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

Product details

Intended Use: Limited to the classification and grading management measures for medical devices, the first level identification range of "red blood cell lytic agent (B.8540)".
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.8540 紅血球溶解劑
Import Information: Chinese goods;; input

Dates and status

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

About this record

Access comprehensive regulatory information for "Shanghai Optoelectronics" erythrocytolytic agent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c26e5cfd27973847a50f98141d6129a5 and manufactured by SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP.. The authorized representative in Taiwan is CHFO BIOMED CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.