TRICELL PRP Kit - Indonesia BPOM Medical Device Registration
TRICELL PRP Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206914854. The device is manufactured by REV-MED INC. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
REV-MED INC.Country of Origin
Korea
Authorized Representative
PT. HARMONI PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Feb 07, 2024
Expiry Date
Dec 12, 2028
Product Type
Manual Hematology Equipment
Platelet aggregometer.
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