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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 31003127311. 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 31003127311

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

Dec 06, 2023

Expiry Date

Mar 31, 2025

Product Type

Therapeutic Neurology Equipment

Neurovascular embolization device.

Non Electromedic Sterile

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