GEISTER Coronary Artery By-Pass Graft Set - Indonesia BPOM Medical Device Registration
GEISTER Coronary Artery By-Pass Graft Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10504212684. The device is manufactured by GEISTER MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDTEK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GEISTER MEDIZINTECHNIK GMBH.Country of Origin
Germany
Authorized Representative
MEDTEKAR Address
DELTA BUILDING BLOK A-11, C-1 & C-2, JL. SURYOPRANOTO NO.1-9, RT/RW 004/007
Registration Date
Oct 07, 2024
Expiry Date
Dec 31, 2026
Product Type
Surgical Cardiology Equipment
Cardiovascular surgical instruments.
Non Electromedic Non Sterile
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