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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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BPOM Registered
Risk Class Kelas Resiko : D
YUKON CC
Analysis ID: AKL 30503814434

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

TRANSLUMINA GMBH.

Country of Origin

Germany

Authorized Representative

PT. HARMONI PRIMA MEDIKA

AR 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

Non Electromedic Sterile

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