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PHIL™ Liquid Embolic System - Indonesia BPOM Medical Device Registration

PHIL™ Liquid Embolic System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31003125430. The device is manufactured by MICROVENTION, INC from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ADMIRAL BLESENSA IMMORTAL.

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BPOM Registered
Risk Class Kelas Resiko : D
PHIL™ Liquid Embolic System
Analysis ID: AKL 31003125430

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

MICROVENTION, INC

Country of Origin

United States

Authorized Representative

PT. ADMIRAL BLESENSA IMMORTAL

AR Address

Ruko Graha Handaya unit H Jl. Raya Pejuangan Kav. 12A, Kebon Jeruk, Kota Jakarta Barat, Kode Pos 11530

Registration Date

Jul 04, 2024

Expiry Date

May 31, 2025

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Electromedic Sterile

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