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BRAILE Cannula for Anterograde Cardioplegia - Indonesia BPOM Medical Device Registration

BRAILE Cannula for Anterograde Cardioplegia is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504320159. The device is manufactured by BRAILE BIOMร‰DICA INDUSTRIA, COMERCIO E REPRESENTACOES LTDA from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MULTIDAYA MEDIKA.

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Risk Class Kelas Resiko : C
BRAILE Cannula for Anterograde Cardioplegia
Analysis ID: AKL 20504320159

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Jun 13, 2023

Expiry Date

Jul 23, 2026

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass vascular catheter, cannula, or tubing.

Non Electromedic Sterile

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