CORPULS3 - Indonesia BPOM Medical Device Registration
CORPULS3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505313601. The device is manufactured by GS ELEKTROMEDIZINISCHE GERรTE GMBH. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
GS ELEKTROMEDIZINISCHE GERรTE GMBH.Country of Origin
Germany
Authorized Representative
PT. SEKARGUNA MEDIKAAR Address
JL. Ciputat Raya Nomor 64
Registration Date
May 13, 2023
Expiry Date
Aug 28, 2027
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
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