NEODENT Titanium Base Abutment - Indonesia BPOM Medical Device Registration

NEODENT Titanium Base Abutment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602520001. The device is manufactured by JJGC INDúSTRIA E COMéRCIO DE MATERIAIS DENTáRIOS SA from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FONDACO JAYATAMA.

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.