REOCOR External Heart Pacemaker - Indonesia BPOM Medical Device Registration
REOCOR External Heart Pacemaker is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503515922. The device is manufactured by BIOTRONIK SE & CO., KG. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOTRONIK SE & CO., KG.Country of Origin
Germany
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Aug 11, 2020
Expiry Date
Jan 28, 2025
Product Type
Prosthetic Cardiology Equipment
External pacemaker pulse generator.
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