VIVEST Automated External Defibrillator - Indonesia BPOM Medical Device Registration
VIVEST Automated External Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320267. The device is manufactured by VIVEST MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is AMPM HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
VIVEST MEDICAL TECHNOLOGY CO.,LTD.Country of Origin
China
Authorized Representative
AMPM HEALTHCARE INDONESIAAR Address
Jl.Cengkeh Kav.16 No.29-30
Registration Date
Sep 07, 2023
Expiry Date
Jan 05, 2026
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
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