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.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 2
Manufacturer
MEDONICA CO., LTD.Country of Origin
Korea
Authorized Representative
PT. MITRAMED FARMA UTAMAAR 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

