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LifeStream Balloon Expandable Vascular Covered Stent - Indonesia BPOM Medical Device Registration

LifeStream Balloon Expandable Vascular Covered Stent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503122420. The device is manufactured by CLEARSTREAM TECHNOLOGIES LTD. from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ITAMA RANORAYA.

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
LifeStream Balloon Expandable Vascular Covered Stent
Analysis ID: AKL 30503122420

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Ireland

Authorized Representative

PT. ITAMA RANORAYA

AR Address

MT Haryono Square Lantai 1 Unit 1, Jl. Otto Iskandardinata Raya No. 390 RT 006 RW 012 Kel. Bidara Cina, Kec. Jatinegara, Jakarta Timur, DKI Jakarta

Registration Date

May 05, 2021

Expiry Date

Nov 09, 2025

Product Type

Prosthetic Cardiology Equipment

Endovascular Graft

Non Electromedic Sterile

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