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VIKAMED Electrocardiograph 3 Channel - Indonesia BPOM Medical Device Registration

VIKAMED Electrocardiograph 3 Channel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502520041. The device is manufactured by EDAN INSTRUMENT., INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
VIKAMED Electrocardiograph 3 Channel
Analysis ID: AKL 20502520041

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

JL. Ciputat Raya Nomor 64

Registration Date

Jan 14, 2025

Expiry Date

Jan 13, 2028

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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