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CLEARVIEW High Pressure Manifold and Adapter - Indonesia BPOM Medical Device Registration

CLEARVIEW High Pressure Manifold and Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501717201. The device is manufactured by UMBRA MEDICAL PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MULTIDAYA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
CLEARVIEW High Pressure Manifold and Adapter
Analysis ID: AKL 20501717201

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MULTIDAYA MEDIKA

AR Address

RUKAN NIAGA GUNUNG SAHARI BLOK B-1

Registration Date

Apr 13, 2021

Expiry Date

Jan 01, 2024

Product Type

Diagnostic Cardiology Equipment

Flow-directed catheter.

Non Electromedic Sterile

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