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NIHON PER CardiofaxS Electrocardiograph - Indonesia BPOM Medical Device Registration

NIHON PER CardiofaxS Electrocardiograph is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502812076. The device is manufactured by SHANGHAI KOHDEN MEDICAL ELECTRONIC INSTRUMENT CORP. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.

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Risk Class Kelas Resiko : B
NIHON PER CardiofaxS Electrocardiograph

NIHON KOHDEN CardiofaxS Electrocardiograph

Analysis ID: AKL 20502812076

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOMEDIK NIAGA PERKASA

AR Address

Jl. Raya Kebayoran Lama No.35 RT.008 RW.001 Kelurahan Sukabumi Selatan, Kecamatan Kebon Jeruk, Jakarta Barat, DKI Jakarta

Registration Date

May 16, 2023

Expiry Date

Mar 31, 2026

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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