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CLEARVIEW Intracoronary Shunt - Indonesia BPOM Medical Device Registration

CLEARVIEW Intracoronary Shunt is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504515945. The device is manufactured by VIANT MEDICAL INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
CLEARVIEW Intracoronary Shunt
Analysis ID: AKL 20504515945

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

VIANT MEDICAL INC.

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Dec 13, 2023

Expiry Date

Feb 06, 2028

Product Type

Surgical Cardiology Equipment

Cardiopulmonary bypass vascular catheter, cannula, or tubing.

Non Electromedic Sterile

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