DIRECTCHECK Whole Blood Control - Indonesia BPOM Medical Device Registration
DIRECTCHECK Whole Blood Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208810532. The device is manufactured by ACCRIVA DIAGNOSTICS INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCRIVA DIAGNOSTICS INC.Country of Origin
United States
Authorized Representative
DEMKA SAKTIAR Address
JLN. TANAH ABANG III/19 A-B, RT.002/RW.003
Registration Date
Nov 01, 2024
Expiry Date
Dec 31, 2028
Product Type
Hematological Reagents
Hematology quality control mixture.
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