DIAGAST ABD Light - Indonesia BPOM Medical Device Registration
DIAGAST ABD Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209701782. The device is manufactured by DIAGAST from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.
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DIAGAST ABD-Lys
Risk Classification
Product Class
Kelas : 2
Manufacturer
DIAGASTCountry of Origin
France
Authorized Representative
PT. MEDQUEST JAYA GLOBALAR Address
Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A
Registration Date
Feb 26, 2023
Expiry Date
Aug 11, 2027
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
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