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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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BPOM Registered
Risk Class Kelas Resiko : C
LEUCOLAB LCG2b
Analysis ID: AKL 20209021156

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MACO PHARMA

Country of Origin

France

Authorized Representative

PT. MEDQUEST JAYA GLOBAL

AR 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.

Non Electromedic Sterile

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