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BOSKA Digital Electrocardiograph 3 Channel - Indonesia BPOM Medical Device Registration

BOSKA Digital Electrocardiograph 3 Channel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420201. The device is manufactured by SHENZHEN LE MEDICAL TECHNOLOGY CO,. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KARUNIAJAYA ANDALAN PRIMA.

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BPOM Registered
Risk Class Kelas Resiko : B
BOSKA Digital Electrocardiograph 3 Channel
Analysis ID: AKL 20502420201

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. KARUNIAJAYA ANDALAN PRIMA

AR Address

Ruko Jalur Sutera Timur 6B No. 23, Alam Sutera , RT.01/RW.15

Registration Date

Jun 13, 2024

Expiry Date

Mar 26, 2027

Product Type

Monitoring Cardiology Equipment

Electrocardiograph.

Non Radiation Electromedics

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