Pure Global

HI-TORQUE Progress 40 Guide Wire - Indonesia BPOM Medical Device Registration

HI-TORQUE Progress 40 Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501612581. 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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
HI-TORQUE Progress 40 Guide Wire
Analysis ID: AKL 20501612581

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

Nov 12, 2019

Expiry Date

Apr 17, 2024

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing