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RHA ™ -Revass Hydrophilic Angiographic Catheter - Indonesia BPOM Medical Device Registration

RHA ™ -Revass Hydrophilic Angiographic Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501910984. The device is manufactured by APT MEDICAL INC. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN REVASS MEDIKA.

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Risk Class Kelas Resiko : C
RHA ™ -Revass Hydrophilic Angiographic Catheter
Analysis ID: AKL 20501910984

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

APT MEDICAL INC.

Country of Origin

China

Authorized Representative

PT. MAIN REVASS MEDIKA

AR Address

Jl. Dewi Sartika No. 4B RT 004/007 Kel. Cililitan Kec. Kramat jati

Registration Date

Apr 04, 2022

Expiry Date

Dec 31, 2024

Product Type

Diagnostic Cardiology Equipment

Diagnostic intravascular catheter.

Non Electromedic Sterile

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