ULTRACARE Diagnostics Anti-AB - Indonesia BPOM Medical Device Registration
ULTRACARE Diagnostics Anti-AB is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320611. The device is manufactured by ULTRACARE CO., LTD. from Egypt, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SAMUDERA INTI MEDISINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ULTRACARE CO., LTD.Country of Origin
Egypt
Authorized Representative
PT. SAMUDERA INTI MEDISINDOAR Address
SAMUDERA INTI MEDISINDO
Registration Date
Sep 03, 2023
Expiry Date
Jan 30, 2027
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
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