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CANON Diagnostic Ultrasound System Aplio i600 - Indonesia BPOM Medical Device Registration

CANON Diagnostic Ultrasound System Aplio i600 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501916877. The device is manufactured by CANON MEDICAL SYSTEMS CORPORATION from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.

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BPOM Registered
Risk Class Kelas Resiko : B
CANON Diagnostic Ultrasound System Aplio i600
Analysis ID: AKL 21501916877

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. MURTI INDAH SENTOSA

AR Address

WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH

Registration Date

May 19, 2020

Expiry Date

Dec 31, 2024

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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