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ALLURE™ RF Cardiac Resynchronization Therapy Device Pulse Generator - Indonesia BPOM Medical Device Registration

ALLURE™ RF Cardiac Resynchronization Therapy Device Pulse Generator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503819486. The device is manufactured by ST. JUDE MEDICAL PUERTO RICO, LLC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : D
ALLURE™ RF Cardiac Resynchronization Therapy Device Pulse Generator
Analysis ID: AKL 30503819486

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

RUKAN PERMATA SENAYAN BLOK A18-19 JL. TENTARA PELAJAR NO. 5

Registration Date

Dec 31, 2018

Expiry Date

Dec 31, 2023

Product Type

Prosthetic Cardiology Equipment

Automatic Implantable Cardioverter Defibrillator With Cardiac Resynchronization (Crt-D)

Non Radiation Electromedics

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