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STENOFLEX Sirolimus Eluting Coronary Stent System - Indonesia BPOM Medical Device Registration

STENOFLEX Sirolimus Eluting Coronary Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503220076. The device is manufactured by KAMAL ENCON INDUSTRIES LIMITED from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL 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.

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BPOM Registered
Risk Class Kelas Resiko : D
STENOFLEX Sirolimus Eluting Coronary Stent System
Analysis ID: AKL 30503220076

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. ANDAMAN MEDICAL INDONESIA

AR Address

Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma

Registration Date

Jul 22, 2022

Expiry Date

Mar 20, 2025

Product Type

Prosthetic Cardiology Equipment

Drug eluting stent

Non Electromedic Sterile

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