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CHRONALIFEMED Handheld Pulse Oximeter - Indonesia BPOM Medical Device Registration

CHRONALIFEMED Handheld Pulse Oximeter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20502420165. The device is manufactured by HUNAN ACCURATE BIO-MEDICAL 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 Handheld Pulse Oximeter
Analysis ID: AKL 20502420165

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

May 02, 2024

Expiry Date

Jan 17, 2029

Product Type

Monitoring Cardiology Equipment

Oximeter.

Non Radiation Electromedics

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