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BEGRAFT Aortic Stent Graft System - Indonesia BPOM Medical Device Registration

BEGRAFT Aortic Stent Graft System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503817499. The device is manufactured by BENTLEY INNOMED GMBH from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is NUGRA KARSERA.

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 : D
BEGRAFT Aortic Stent Graft System
Analysis ID: AKL 30503817499

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Oct 10, 2024

Expiry Date

Dec 31, 2028

Product Type

Prosthetic Cardiology Equipment

Coronary stent

Non Electromedic Sterile

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