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H-STENT™ Coronary Stent Delivery System - Indonesia BPOM Medical Device Registration

H-STENT™ Coronary Stent Delivery System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503320279. The device is manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CEKINDO BUSINESS INTERNATIONAL.

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
H-STENT™ Coronary Stent Delivery System
Analysis ID: AKL 30503320279

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. CEKINDO BUSINESS INTERNATIONAL

AR Address

CEKINDO BUSINESS INTERNATIONAL

Registration Date

Sep 07, 2023

Expiry Date

Dec 31, 2027

Product Type

Prosthetic Cardiology Equipment

Coronary stent

Non Electromedic Sterile

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