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AVISO S Ultrasound Platform - Indonesia BPOM Medical Device Registration

AVISO S Ultrasound Platform is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501615842. The device is manufactured by QUANTEL MEDICAL. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURYA TAMA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
AVISO S Ultrasound Platform
Analysis ID: AKL 21501615842

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

QUANTEL MEDICAL.

Country of Origin

France

Authorized Representative

PT. SURYA TAMA MEDIKA

AR Address

Jl m hasibuan ruko suncity pbb. 37 real blok e.27 rt 004 rw 002 kel margajaya kec bekasi selatan kota bekasi

Registration Date

Aug 24, 2020

Expiry Date

Feb 12, 2024

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed echo imaging system.

Non Radiation Electromedics

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