MISONIX SONASTAR Ultrasonic Surgical Aspiration Sy - Indonesia BPOM Medical Device Registration

MISONIX SONASTAR Ultrasonic Surgical Aspiration Sy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21303611446. The device is manufactured by MISONIX INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SIGMA KARSA MAGNA.

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.