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MCI System Instruments - Indonesia BPOM Medical Device Registration

MCI System Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10602420019. The device is manufactured by MCI - MEDICAL CONCEPT INNOVATION INC from United States, and is classified as Risk Class Kelas Resiko : A. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
MCI System Instruments
Analysis ID: AKL 10602420019

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

KIMERA FLUX INDONESIA

AR Address

Ruko Melati Vista V21/A2 Jl.Boulevard

Registration Date

Jan 16, 2024

Expiry Date

Mar 03, 2028

Product Type

Prosthetic Dental Equipment

Endosseous dental implant accessories.

Non Electromedic Non Sterile

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