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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
BENTLEY INNOMED GMBHCountry of Origin
Germany
Authorized Representative
NUGRA KARSERAAR 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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