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MEDONICA Mobile X-Ray System - Indonesia BPOM Medical Device Registration

MEDONICA Mobile X-Ray System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501713409. The device is manufactured by MEDONICA CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRAMED FARMA UTAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
MEDONICA Mobile X-Ray System
Analysis ID: AKL 21501713409

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDONICA CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. MITRAMED FARMA UTAMA

AR Address

PATRA OFFICE TOWER LANTAI XVII, RUANG 1702, JL. JENDRAL GATOT SUBROTO KAV. 32-34

Registration Date

Aug 10, 2021

Expiry Date

Apr 01, 2026

Product Type

Diagnostic Radiology Equipment

Mobile x-ray system.

Electromedic Radiation

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