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BRAILE Non-Wirewound Arterial Cannula - Indonesia BPOM Medical Device Registration

BRAILE Non-Wirewound Arterial Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501912002. The device is manufactured by BRAILE BIOMÉDICA INDUSTRIA, COMERCIO E REPRESENTACOES LTDA from Brazil, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
BRAILE Non-Wirewound Arterial Cannula
Analysis ID: AKL 20501912002

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Aug 05, 2021

Expiry Date

Jul 23, 2026

Product Type

Diagnostic Cardiology Equipment

Catheter cannula.

Non Electromedic Sterile

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