CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH - Indonesia BPOM Medical Device Registration

CARTO VIZIGO BI-DIRECTIONAL GUIDING SHEATH is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501817995. The device is manufactured by FREUDENBERG MEDICAL LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON NEW ZEALAND.

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.