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HI-TORQUE VERSATURN Guide Wire - Indonesia BPOM Medical Device Registration

HI-TORQUE VERSATURN Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501123657. The device is manufactured by ABBOTT VASCULAR from Puerto Rico USA, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ABBOTT PRODUCTS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
HI-TORQUE VERSATURN Guide Wire
Analysis ID: AKL 20501123657

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ABBOTT VASCULAR

Country of Origin

Puerto Rico USA

Authorized Representative

PT. ABBOTT PRODUCTS INDONESIA

AR Address

WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA

Registration Date

Dec 06, 2022

Expiry Date

Sep 11, 2025

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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