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PAP Defibrillator Monitor - Indonesia BPOM Medical Device Registration

PAP Defibrillator Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505220041. The device is manufactured by SHENZEN COMEN MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. FLUORESCENT ANDHIKA PARAMARTHA.

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BPOM Registered
Risk Class Kelas Resiko : D
PAP Defibrillator Monitor
Analysis ID: AKL 30505220041

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. FLUORESCENT ANDHIKA PARAMARTHA

AR Address

RUKAN GADING BUKIT INDAH BLOK U / 09 RT 008 RW 015 - KOMPLEK GADING BUKIT INDAH - JL. BUKIT INDAH RAYA KELAPA GADING JAKARTA UTARA

Registration Date

Apr 27, 2022

Expiry Date

Apr 20, 2025

Product Type

Therapeutic Cardiology Equipment

Automated external defibrillator.

Non Radiation Electromedics

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