LIFEPAK 20e Defibrillator/Monitor - Indonesia BPOM Medical Device Registration

LIFEPAK 20e Defibrillator/Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505612563. The device is manufactured by PHYSIO CONTROL INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : D

LIFEPAK 20e Defibrillator/Monitor

Analysis ID: AKL 30505612563

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

PHYSIO CONTROL INC.

Country of Origin

United States

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Feb 22, 2023

Expiry Date

Mar 31, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

DJ Fang

MedTech Regulatory Expert

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