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MEDTRONIC Angiographic Guide Wire - Indonesia BPOM Medical Device Registration

MEDTRONIC Angiographic Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501412952. The device is manufactured by MEDTRONIC VASCULAR 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
MEDTRONIC Angiographic Guide Wire
Analysis ID: AKL 20501412952

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

MEDTRONIC VASCULAR

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Sep 24, 2020

Expiry Date

Mar 12, 2025

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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