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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.

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Risk Class Kelas Resiko : C
MEMBRANE OXYGENATOR OXYPRIME DUO
Analysis ID: AKL 20504420084

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jun 24, 2024

Expiry Date

Feb 01, 2029

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass oxygenator.

Non Electromedic Sterile

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