LIQUICHEK D-dimer Control - Indonesia BPOM Medical Device Registration
LIQUICHEK D-dimer Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208320658. The device is manufactured by BIORAD LABROATORIES INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIASTIKA BIOTEKINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BIORAD LABROATORIES INC.Country of Origin
United States
Authorized Representative
DIASTIKA BIOTEKINDOAR Address
Rukan Sentra Pemuda Kav.30 - 31 Jalan Pemuda No.61 RT.009 RW.003 Kel. Rawamangun Kec.Pulogadung
Registration Date
Aug 01, 2023
Expiry Date
May 31, 2025
Product Type
Hematological Reagents
Hematology quality control mixture.
Invitro Diagnostics
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LIQUICHECK Immunoassay Plus Control Level 2
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