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CHRONALIFEMED Patient Monitor - Indonesia BPOM Medical Device Registration

CHRONALIFEMED Patient Monitor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420221. The device is manufactured by JIANGSU KONSUNG BIO-MEDICAL SCIENCE AND TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BUANA INTIPRIMA USAHA.

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BPOM Registered
Risk Class Kelas Resiko : B
CHRONALIFEMED Patient Monitor
Analysis ID: AKL 20502420221

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. BUANA INTIPRIMA USAHA

AR Address

GUDANG THE STORE AT GREEN LAKE CITY CLUSTER GUDANG RCTS NOMOR 50

Registration Date

Jun 28, 2024

Expiry Date

Jun 26, 2027

Product Type

Monitoring Cardiology Equipment

Cardiac monitor (including cardiotachometer and rate alarm).

Non Electromedic Non Sterile

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