SOPROCARE ROOM S950 - Indonesia BPOM Medical Device Registration

SOPROCARE ROOM S950 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20601814203. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DENTALITIES GROUP ASIA.

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.