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BEXEN Defibrillator Monitor - Indonesia BPOM Medical Device Registration

BEXEN Defibrillator Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505413307. The device is manufactured by OSATU S COOP. from Spain, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTEK.

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BPOM Registered
Risk Class Kelas Resiko : D
BEXEN Defibrillator Monitor
Analysis ID: AKL 30505413307

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

OSATU S COOP.

Country of Origin

Spain

Authorized Representative

PT. MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Apr 08, 2020

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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