HEMOCHRON Celite ACT Tubes - Indonesia BPOM Medical Device Registration
HEMOCHRON Celite ACT Tubes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101712453. 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 PT. DEMKA SAKTI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCRIVA DIAGNOSTICS INC.Country of Origin
United States
Authorized Representative
PT. DEMKA SAKTIAR Address
Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat
Registration Date
Jun 28, 2021
Expiry Date
Dec 31, 2024
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
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