Taiwan FDA registration 3678496cfce8c5c29787101ff0baf9fb

"Bio-Rad" EQAS ToRCH/EBV/MuMZ Program (non-sterile)

TW: "伯瑞" 血清病原體外部品保計畫 (未滅菌)

Taiwan·Risk Class 1·MD·BIO-RAD LABORATORIES·Registered Jul 05, 2016 – Jul 05, 2026Expired

Registration details

Analysis ID: 3678496cfce8c5c29787101ff0baf9fb
License Form: Ministry of Health Medical Device Import No. 016739
Customs Code: DHA09401673902

Company information

Manufacturer: BIO-RAD LABORATORIES
Manufacturer Country: United States
Authorized Representative: Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.)

Product details

Intended Use: Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information: Imported from abroad; GMP

Dates and status

Registration Date: Jul 05, 2016
Expiry Date: Jul 05, 2026

About this record

Access comprehensive regulatory information for "Bio-Rad" EQAS ToRCH/EBV/MuMZ Program (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3678496cfce8c5c29787101ff0baf9fb and manufactured by BIO-RAD LABORATORIES. The authorized representative in Taiwan is Bio-Rad Laboratories Inc., Taiwan Branch (U.S.A.).

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