RED CELL AHG GEL CARD - Indonesia BPOM Medical Device Registration
RED CELL AHG GEL CARD is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209024820. The device is manufactured by RED CELL BIYOTEKNOLOJI A.S from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PANJI PRIMA DINAMIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RED CELL BIYOTEKNOLOJI A.SCountry of Origin
Turkey
Authorized Representative
PT. PANJI PRIMA DINAMIKAAR Address
Jalan Kalibata Timur III No. 55 Kalibata, Pancoran
Registration Date
Feb 06, 2025
Expiry Date
Sep 26, 2029
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated Coombs test systems.
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