COROFLEX ISAR NEO Coronary Stent System - Indonesia BPOM Medical Device Registration
COROFLEX ISAR NEO Coronary Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503713308. The device is manufactured by B BRAUN MELSUNGEN AG. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
B BRAUN MELSUNGEN AG.Country of Origin
Germany
Authorized Representative
B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Sep 21, 2023
Expiry Date
Aug 18, 2027
Product Type
Prosthetic Cardiology Equipment
Drug eluting stent
Non Electromedic Sterile
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