KERR VERTISE FLOW - Indonesia BPOM Medical Device Registration

KERR VERTISE FLOW is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602420405. The device is manufactured by KERR CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TIGASATU MEDIKA SOLUSINDO.

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.