REDCELL LISS DILUENT - Indonesia BPOM Medical Device Registration
REDCELL LISS DILUENT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209024913. The device is manufactured by RED CELL BIYOKTEKNOLOJI A.S from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PANJI PRIMA DINAMIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RED CELL BIYOKTEKNOLOJI A.SCountry of Origin
Turkey
Authorized Representative
PANJI PRIMA DINAMIKAAR Address
Jalan Kalibata Timur III No. 55 Kalibata, Pancoran
Registration Date
Feb 06, 2025
Expiry Date
Dec 30, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
Invitro Diagnostics

