RAMP 200 System and Accessories - Indonesia BPOM Medical Device Registration
RAMP 200 System and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304910776. 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 FAITHFUL MEDICAL GRACE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
RESPONSE BIOMEDICAL CORPORATION.Country of Origin
Canada
Authorized Representative
FAITHFUL MEDICAL GRACEAR Address
Mitra Sunter Boulevard Blok B No.39 Jl. Yos Sudarso Kav. 89
Registration Date
Apr 06, 2022
Expiry Date
Jan 21, 2027
Product Type
Immunology Laboratory Equipment and Reagents
Immunofluorometer equipment
Invitro Diagnostics
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RAMP Procalcitonin Controls Level 2
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RAMP Myoglobin Assay
RAMP CK-MB Assay
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