LEUCOLAB LCG2b - Indonesia BPOM Medical Device Registration
LEUCOLAB LCG2b is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209021156. The device is manufactured by MACO PHARMA 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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Risk Classification
Product Class
Kelas : 2
Manufacturer
MACO PHARMACountry of Origin
France
Authorized Representative
PT. MEDQUEST JAYA GLOBALAR Address
Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A
Registration Date
Mar 17, 2020
Expiry Date
Dec 10, 2024
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Empty container for the collection and processing of blood and blood components.
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