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MINDRAY BENEHEART D2 Defibrillator / Monitor - Indonesia BPOM Medical Device Registration

MINDRAY BENEHEART D2 Defibrillator / Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505715439. The device is manufactured by SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MINDRAY MEDICAL INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
MINDRAY BENEHEART D2 Defibrillator / Monitor
Analysis ID: AKL 30505715439

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. MINDRAY MEDICAL INDONESIA

AR Address

Menara DEA II Lt.17, Jl. Mega Kuningan Barat Kav.E4.3 No.1-2, Kel. Kuningan Timur, Kec.Setiabudi Kawasan Mega Kuningan, Jakarta Selatan

Registration Date

May 17, 2021

Expiry Date

Nov 02, 2025

Product Type

Therapeutic Cardiology Equipment

DC-defibrillator (including paddles).

Non Radiation Electromedics

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