TriCell PRP L - Indonesia BPOM Medical Device Registration
TriCell PRP L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206917835. 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 HARMONY PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
REV-MED INC.Country of Origin
Korea
Authorized Representative
HARMONY PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Nov 29, 2019
Expiry Date
Mar 23, 2024
Product Type
Manual Hematology Equipment
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