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LEO+ Intracranial Self Expandable Stent and Delivery System - Indonesia BPOM Medical Device Registration

LEO+ Intracranial Self Expandable Stent and Delivery System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003711652. The device is manufactured by BALT EXTRUSION SAS from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDIKON MAIN PHARMALAB.

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Risk Class Kelas Resiko : D
LEO+ Intracranial Self Expandable Stent and Delivery System
Analysis ID: AKL 31003711652

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BALT EXTRUSION SAS

Country of Origin

France

Authorized Representative

PT. MEDIKON MAIN PHARMALAB

AR Address

JLN. RAYA PASAR MINGGU NO 15, RT.001/07

Registration Date

Oct 30, 2024

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Electromedic Sterile

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