PUREMED Medical Oxygen Regulator - Indonesia BPOM Medical Device Registration

PUREMED Medical Oxygen Regulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10402420039. The device is manufactured by DANYANG AIRTECH CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROYAL SEJAHTERA MANDIRI.

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.