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FLIXENE Vascular Graft - Indonesia BPOM Medical Device Registration

FLIXENE Vascular Graft is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503811243. The device is manufactured by ATRIUM MEDICAL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MAGENTA BIOMEDIKA.

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 : C
FLIXENE Vascular Graft
Analysis ID: AKL 20503811243

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

MAGENTA BIOMEDIKA

AR Address

Ruko Buaran Persada No. 30, Jl. Raya Soekamto, Duren Sawit

Registration Date

Dec 07, 2023

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Cardiology Equipment

Vascular graft prosthesis.

Non Electromedic Sterile

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