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SONOSCANNER Ultrasound Scanner - Indonesia BPOM Medical Device Registration

SONOSCANNER Ultrasound Scanner is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420740. The device is manufactured by SONOSCANNER SARL from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PETAN DAYA MEDICA.

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BPOM Registered
Risk Class Kelas Resiko : B
SONOSCANNER Ultrasound Scanner
Analysis ID: AKL 21501420740

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SONOSCANNER SARL

Country of Origin

France

Authorized Representative

PT. PETAN DAYA MEDICA

AR Address

Komplek Setia Budi Point Jl. Setia Budi Blok C No. 3-4 Medan

Registration Date

Oct 23, 2024

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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