VERIFYNOW PRUTest Platelet Reactivity Test - Indonesia BPOM Medical Device Registration
VERIFYNOW PRUTest Platelet Reactivity Test is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20205121138. 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 HARMONY PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ACCRIVA DIAGNOSTICS, INC.Country of Origin
United States
Authorized Representative
HARMONY PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Oct 16, 2024
Expiry Date
Oct 01, 2029
Product Type
Automatic and Semi-Automatic Hematology Equipment
Automated platelet aggregation system.
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