YUKON CC - Indonesia BPOM Medical Device Registration
YUKON CC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503814434. The device is manufactured by TRANSLUMINA GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
TRANSLUMINA GMBH.Country of Origin
Germany
Authorized Representative
PT. HARMONI PRIMA MEDIKAAR Address
Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150
Registration Date
Dec 10, 2020
Expiry Date
Oct 26, 2025
Product Type
Prosthetic Cardiology Equipment
Coronary stent
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