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FEAS ELECTRONICA Defibrillator Monitor 3850B - Indonesia BPOM Medical Device Registration

FEAS ELECTRONICA Defibrillator Monitor 3850B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505711623. The device is manufactured by FEAS ELECTRONICA SA. from Argentina, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BINTANG SARANA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
FEAS ELECTRONICA Defibrillator Monitor 3850B
Analysis ID: AKL 30505711623

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Argentina

Authorized Representative

PT. BINTANG SARANA MEDIKA

AR Address

KOMPLEK RUKAN MEDIKAL E/2 RT 001 RW 001 KELURAHAN PONDOK KELAPA KECAMATAN DUREN SAWIT 13450

Registration Date

Sep 21, 2022

Expiry Date

Mar 23, 2027

Product Type

Therapeutic Cardiology Equipment

DC-defibrillator (including paddles).

Non Radiation Electromedics

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