MCI CMF System - Indonesia BPOM Medical Device Registration
MCI CMF System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603320743. The device is manufactured by MCI - MEDICAL CONCEPT INNOVATION INC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is KIMERA FLUX INDONESIA.
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
MCI - MEDICAL CONCEPT INNOVATION INCCountry of Origin
United States
Authorized Representative
KIMERA FLUX INDONESIAAR Address
Ruko Melati Vista V21/A2 Jl.Boulevard
Registration Date
Oct 17, 2023
Expiry Date
Mar 04, 2028
Product Type
Surgical Dental Equipment
Bone plate.
Non Electromedic Non Sterile

