MEMBRANE OXYGENATOR OXYPRIME DUO - Indonesia BPOM Medical Device Registration
MEMBRANE OXYGENATOR OXYPRIME DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420084. The device is manufactured by BRAILE BIOMÉDICA INDÍSTRIA COMéRCIO E REPRESENTAÇÕES LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.
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.
Risk Classification
Product Class
Kelas : 2
Country of Origin
Brazil
Authorized Representative
PT. MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Jun 24, 2024
Expiry Date
Feb 01, 2029
Product Type
Surgical Cardiology Equipment
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