RAMP Procalcitonin Controls Level 2 - Indonesia BPOM Medical Device Registration
RAMP Procalcitonin Controls Level 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303910053. The device is manufactured by RESPONSE BIOMEDICAL CORPORATION. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RESPONSE BIOMEDICAL CORPORATION.Country of Origin
Canada
Authorized Representative
PT. FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Apr 05, 2022
Expiry Date
Jan 21, 2027
Product Type
Serological Reagents
Device to detect and measure non-microbial analyte(s) in human clinical specimens to aid in assessment of patients with suspected sepsis
Invitro Diagnostics
RAMP Reader System and Accessories
RAMP Cardiac Controls Level 2
RAMP Procalcitonin Controls Level 1
RAMP 200 System and Accessories
RAMP NT-proBNP Assay
RESPONSE RAMP D-dimer
RAMP Myoglobin Assay
RAMP CK-MB Assay
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